Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the endocrine system (HP:0000818)help
Parent Node:
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Abnormal circulating hormone concentration (HP:0003117)help
..Starting node
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Abnormal circulating androgen level (HP:0030347)help
Term ID: 30347
Name: Abnormal circulating androgen level
Synonym:
Definition: An anomaly in the blood concentration of an androgen, that is, of a steroid hormone that controls development and maintenance of masculine characteristics. The androgens include testosterone and Dehydroepiandrosterone.
Comments:
Reference: HP:0030347
Genes and Diseases:
 
       Child Nodes:
........expandAbnormal serum testosterone level (HP:0030087) help
................... HP:0030088 Increased serum testosterone level
................... HP:0040171 Decreased serum testosterone level
........expandIncreased circulating androgen level (HP:0030348) help
................... HP:0025380 Increased serum androstenedione
................... HP:0030088 Increased serum testosterone level
........expandDecreased circulating androgen level (HP:0030349) help
................... HP:0040171 Decreased serum testosterone level
........expandAbnormal serum dehydroepiandrosterone level (HP:0500022) help

 Sister Nodes: 
..expandAbnormal adiponectin level (HP:0030684) help
..expandAbnormal circulating adrenocorticotropin concentration (HP:0011043) help
..expandAbnormal circulating antimullerian hormone concentration (HP:0031101) help
..expandAbnormal circulating estrogen level (HP:0025132) help
..expandAbnormal circulating gonadotropin concentration (HP:0030338) help
..expandAbnormal circulating inhibin level (HP:0031099) help
..expandAbnormal circulating insulin concentration (HP:0040214) help
..expandAbnormal circulating leptin concentration (HP:0004361) help
..expandAbnormal circulating osteocalcin level (HP:0031427) help
..expandAbnormal circulating pregnenolone concentration (HP:0031187) help
..expandAbnormal circulating progesterone level (HP:0031212) help
..expandAbnormal circulating thyroid hormone concentration (HP:0031508) help
..expandAbnormal glucagon level (HP:0030687) help
..expandAbnormal gonadotropin-releasing hormone concentration (HP:0500012) help
..expandAbnormal serum insulin-like growth factor 1 level (HP:0030352) help
..expandAbnormality of circulating catecholamine level (HP:0012099) help
..expandAbnormality of circulating glucocorticoid level (HP:0012111) help
..expandDecreased circulating dehydroepiandrosterone concentration (HP:0031214) help
..expandDecreased circulating dehydroepiandrosterone-sulfate concentration (HP:0031215) help
..expandDecreased circulating parathyroid hormone level (HP:0031817) help
..expandDecreased response to growth hormone stimulation test (HP:0000824) help
..expandElevated circulating parathyroid hormone level (HP:0003165) help
..expandElevated vascular endothelial growth factor level (HP:0031052) help
..expandFasting hypoglycemia (HP:0003162) help
..expandIncreased pituitary glycoprotein hormone alpha subunit level (HP:0031208) help
..expandIncreased serum serotonin (HP:0003144) help
..expandobsolete Increased serum 1,25-dihydroxyvitamin D3 (HP:0003152) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030347HP:0030347Abnormal circulating androgen level0AKT1 CL E G H207391ORPHA:2495Meningioma54
HP:0030347HP:0030347Abnormal circulating androgen level0ALG6 CL E G H2992923157ORPHA:79320ALG6-CDG66
HP:0030347HP:0030347Abnormal circulating androgen level0ALMS1 CL E G H7840428ORPHA:64Alström syndrome404
HP:0030347HP:0030347Abnormal circulating androgen level0ANOS1 CL E G H37306211OMIM:308700Hypogonadotropic hypogonadism 1 with or without anosmia65
HP:0030347HP:0030347Abnormal circulating androgen level0AR CL E G H367644ORPHA:99429Complete androgen insensitivity syndrome125
HP:0030347HP:0030347Abnormal circulating androgen level0AR CL E G H367644ORPHA:90797Partial androgen insensitivity syndrome125
HP:0030347HP:0030347Abnormal circulating androgen level0B4GALNT1 CL E G H25834117ORPHA:101006Autosomal recessive spastic paraplegia type 2625
HP:0030347HP:0030347Abnormal circulating androgen level0B4GALNT1 CL E G H25834117OMIM:609195Spastic paraplegia 26, autosomal recessive25
HP:0030347HP:0030347Abnormal circulating androgen level0BAP1 CL E G H8314950ORPHA:2495Meningioma184
HP:0030347HP:0030347Abnormal circulating androgen level0BMP6 CL E G H6541073ORPHA:465508Symptomatic form of hemochromatosis type 1
HP:0030347HP:0030347Abnormal circulating androgen level0CDKN2A CL E G H10291787ORPHA:1501Adrenocortical carcinoma289
HP:0030347HP:0030347Abnormal circulating androgen level0CHD7 CL E G H5563620626ORPHA:432Normosmic congenital hypogonadotropic hypogonadism515
HP:0030347HP:0030347Abnormal circulating androgen level0CLN3 CL E G H12012074ORPHA:228346CLN3 disease216
HP:0030347HP:0030347Abnormal circulating androgen level0CPE CL E G H13632303OMIM:619326BDV SYNDROME; BDVS
HP:0030347HP:0030347Abnormal circulating androgen level0CTNNB1 CL E G H14992514ORPHA:1501Adrenocortical carcinoma88
HP:0030347HP:0030347Abnormal circulating androgen level0CYB5A CL E G H15282570ORPHA:9079646,XY disorder of sex development due to isolated 17,20-lyase deficiency2
HP:0030347HP:0030347Abnormal circulating androgen level0CYP11A1 CL E G H15832590ORPHA:16855846,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency31
HP:0030347HP:0030347Abnormal circulating androgen level0CYP11A1 CL E G H15832590ORPHA:289548Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency31
HP:0030347HP:0030347Abnormal circulating androgen level0CYP11B1 CL E G H15842591OMIM:202010Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency112
HP:0030347HP:0030347Abnormal circulating androgen level0CYP11B1 CL E G H15842591ORPHA:90795Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency112
HP:0030347HP:0030347Abnormal circulating androgen level0CYP17A1 CL E G H15862593ORPHA:9079646,XY disorder of sex development due to isolated 17,20-lyase deficiency53
HP:0030347HP:0030347Abnormal circulating androgen level0CYP17A1 CL E G H15862593ORPHA:90793Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency53
HP:0030347HP:0030347Abnormal circulating androgen level0DCAF17 CL E G H8006725784OMIM:241080Woodhouse-Sakati syndrome87
HP:0030347HP:0030347Abnormal circulating androgen level0DCAF17 CL E G H8006725784ORPHA:3464Woodhouse-Sakati syndrome87
HP:0030347HP:0030347Abnormal circulating androgen level0DHH CL E G H508462865ORPHA:16856346,XY gonadal dysgenesis-motor and sensory neuropathy syndrome21
HP:0030347HP:0030347Abnormal circulating androgen level0DHX37 CL E G H5764717210OMIM:27325046, XY sex reversal 112
HP:0030347HP:0030347Abnormal circulating androgen level0DHX37 CL E G H5764717210ORPHA:25151046,XY partial gonadal dysgenesis2
HP:0030347HP:0030347Abnormal circulating androgen level0DMRT3 CL E G H5852413909ORPHA:25151046,XY partial gonadal dysgenesis1
HP:0030347HP:0030347Abnormal circulating androgen level0DMXL2 CL E G H233122938ORPHA:453533Polyendocrine-polyneuropathy syndrome3
HP:0030347HP:0030347Abnormal circulating androgen level0DUSP6 CL E G H18483072ORPHA:432Normosmic congenital hypogonadotropic hypogonadism4
HP:0030347HP:0030347Abnormal circulating androgen level0FGD1 CL E G H22453663OMIM:305400Aarskog-Scott syndrome62
HP:0030347HP:0030347Abnormal circulating androgen level0FGF17 CL E G H88223673ORPHA:432Normosmic congenital hypogonadotropic hypogonadism3
HP:0030347HP:0030347Abnormal circulating androgen level0FGF8 CL E G H22533686ORPHA:432Normosmic congenital hypogonadotropic hypogonadism17
HP:0030347HP:0030347Abnormal circulating androgen level0FGFR1 CL E G H22603688ORPHA:432Normosmic congenital hypogonadotropic hypogonadism172
HP:0030347HP:0030347Abnormal circulating androgen level0FSHB CL E G H24883964ORPHA:52901Isolated follicle stimulating hormone deficiency23
HP:0030347HP:0030347Abnormal circulating androgen level0FSHR CL E G H24923969ORPHA:64739Ovarian hyperstimulation syndrome50
HP:0030347HP:0030347Abnormal circulating androgen level0GATA4 CL E G H26264173ORPHA:25151046,XY partial gonadal dysgenesis87
HP:0030347HP:0030347Abnormal circulating androgen level0GCNA CL E G H9395315805OMIM:301077SPERMATOGENIC FAILURE, X-LINKED, 4; SPGFX4
HP:0030347HP:0030347Abnormal circulating androgen level0GNAS CL E G H27784392ORPHA:562McCune-Albright syndrome101
HP:0030347HP:0030347Abnormal circulating androgen level0GNRH1 CL E G H27964419OMIM:614841Hypogonadotropic hypogonadism 12 with or without anosmia15
HP:0030347HP:0030347Abnormal circulating androgen level0GNRH1 CL E G H27964419ORPHA:432Normosmic congenital hypogonadotropic hypogonadism15
HP:0030347HP:0030347Abnormal circulating androgen level0GNRHR CL E G H27984421ORPHA:432Normosmic congenital hypogonadotropic hypogonadism92
HP:0030347HP:0030347Abnormal circulating androgen level0HFE CL E G H30774886ORPHA:465508Symptomatic form of hemochromatosis type 138
HP:0030347HP:0030347Abnormal circulating androgen level0HS6ST1 CL E G H93945201ORPHA:432Normosmic congenital hypogonadotropic hypogonadism8
HP:0030347HP:0030347Abnormal circulating androgen level0HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency34
HP:0030347HP:0030347Abnormal circulating androgen level0INSR CL E G H36436091ORPHA:769Rabson-Mendenhall syndrome229
HP:0030347HP:0030347Abnormal circulating androgen level0KISS1 CL E G H38146341ORPHA:432Normosmic congenital hypogonadotropic hypogonadism3
HP:0030347HP:0030347Abnormal circulating androgen level0KISS1R CL E G H846344510ORPHA:432Normosmic congenital hypogonadotropic hypogonadism14
HP:0030347HP:0030347Abnormal circulating androgen level0LEP CL E G H39526553ORPHA:66628Obesity due to congenital leptin deficiency47
HP:0030347HP:0030347Abnormal circulating androgen level0LEPR CL E G H39536554ORPHA:179494Obesity due to leptin receptor gene deficiency46
HP:0030347HP:0030347Abnormal circulating androgen level0LGR4 CL E G H5536613299OMIM:619613DELAYED PUBERTY, SELF-LIMITED; DPSL1
HP:0030347HP:0030347Abnormal circulating androgen level0LHB CL E G H39726584OMIM:228300Hypogonadotropic hypogonadism 23 without anosmia9
HP:0030347HP:0030347Abnormal circulating androgen level0MAP3K1 CL E G H42146848ORPHA:25151046,XY partial gonadal dysgenesis13
HP:0030347HP:0030347Abnormal circulating androgen level0MC2R CL E G H41586930ORPHA:361Familial glucocorticoid deficiency94
HP:0030347HP:0030347Abnormal circulating androgen level0MRAP CL E G H562461304ORPHA:361Familial glucocorticoid deficiency26
HP:0030347HP:0030347Abnormal circulating androgen level0NDNF CL E G H7962526256OMIM:618841HYPOGONADOTROPIC HYPOGONADISM 25 WITH ANOSMIA; HH25
HP:0030347HP:0030347Abnormal circulating androgen level0NF2 CL E G H47717773ORPHA:2495Meningioma220
HP:0030347HP:0030347Abnormal circulating androgen level0NFKB2 CL E G H47917795ORPHA:293978Deficiency in anterior pituitary function-variable immunodeficiency syndrome11
HP:0030347HP:0030347Abnormal circulating androgen level0NNT CL E G H235307863ORPHA:361Familial glucocorticoid deficiency13
HP:0030347HP:0030347Abnormal circulating androgen level0NR0B1 CL E G H1907960ORPHA:25151046,XY partial gonadal dysgenesis48
HP:0030347HP:0030347Abnormal circulating androgen level0NR2F2 CL E G H70267976OMIM:61890146,XX SEX REVERSAL 5; SRXX513
HP:0030347HP:0030347Abnormal circulating androgen level0NR3C1 CL E G H29087978ORPHA:786Generalized glucocorticoid resistance syndrome79
HP:0030347HP:0030347Abnormal circulating androgen level0NR5A1 CL E G H25167983ORPHA:25151046,XY partial gonadal dysgenesis38
HP:0030347HP:0030347Abnormal circulating androgen level0NSMF CL E G H2601229843ORPHA:432Normosmic congenital hypogonadotropic hypogonadism6
HP:0030347HP:0030347Abnormal circulating androgen level0PDGFB CL E G H51558800ORPHA:2495Meningioma9
HP:0030347HP:0030347Abnormal circulating androgen level0PIK3CA CL E G H52908975ORPHA:2495Meningioma162
HP:0030347HP:0030347Abnormal circulating androgen level0POLA1 CL E G H54229173ORPHA:163976X-linked intellectual disability, Van Esch type2
HP:0030347HP:0030347Abnormal circulating androgen level0POLR3A CL E G H1112830074OMIM:264090Wiedemann-Rautenstrauch syndrome138
HP:0030347HP:0030347Abnormal circulating androgen level0POLR3A CL E G H1112830074ORPHA:3455Wiedemann-Rautenstrauch syndrome138
HP:0030347HP:0030347Abnormal circulating androgen level0POR CL E G H54479208ORPHA:95699Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency76
HP:0030347HP:0030347Abnormal circulating androgen level0PRKAR1A CL E G H55739388ORPHA:1501Adrenocortical carcinoma134
HP:0030347HP:0030347Abnormal circulating androgen level0PRKAR1A CL E G H55739388OMIM:610489Pigmented nodular adrenocortical disease, primary, 1134
HP:0030347HP:0030347Abnormal circulating androgen level0PROK2 CL E G H6067518455ORPHA:432Normosmic congenital hypogonadotropic hypogonadism9
HP:0030347HP:0030347Abnormal circulating androgen level0PROKR2 CL E G H12867415836ORPHA:432Normosmic congenital hypogonadotropic hypogonadism34
HP:0030347HP:0030347Abnormal circulating androgen level0RBM28 CL E G H5513121863ORPHA:157954ANE syndrome1
HP:0030347HP:0030347Abnormal circulating androgen level0SEMA3A CL E G H1037110723OMIM:614897Hypogonadotropic hypogonadism 16 with or without anosmia14
HP:0030347HP:0030347Abnormal circulating androgen level0SLC39A4 CL E G H5563017129OMIM:201100Acrodermatitis enteropathica, Zinc-Deficiency type55
HP:0030347HP:0030347Abnormal circulating androgen level0SMARCB1 CL E G H659811103ORPHA:2495Meningioma87
HP:0030347HP:0030347Abnormal circulating androgen level0SMARCE1 CL E G H660511109ORPHA:2495Meningioma47
HP:0030347HP:0030347Abnormal circulating androgen level0SMO CL E G H660811119ORPHA:2495Meningioma22
HP:0030347HP:0030347Abnormal circulating androgen level0SOX9 CL E G H666211204ORPHA:25151046,XY partial gonadal dysgenesis109
HP:0030347HP:0030347Abnormal circulating androgen level0SPRY4 CL E G H8184815533ORPHA:432Normosmic congenital hypogonadotropic hypogonadism5
HP:0030347HP:0030347Abnormal circulating androgen level0SRY CL E G H673611311ORPHA:177245,X/46,XY mixed gonadal dysgenesis23
HP:0030347HP:0030347Abnormal circulating androgen level0SRY CL E G H673611311ORPHA:25151046,XY partial gonadal dysgenesis23
HP:0030347HP:0030347Abnormal circulating androgen level0STAR CL E G H677011359ORPHA:361Familial glucocorticoid deficiency45
HP:0030347HP:0030347Abnormal circulating androgen level0SUFU CL E G H5168416466ORPHA:2495Meningioma124
HP:0030347HP:0030347Abnormal circulating androgen level0TAC3 CL E G H686611521ORPHA:432Normosmic congenital hypogonadotropic hypogonadism6
HP:0030347HP:0030347Abnormal circulating androgen level0TACR3 CL E G H687011528ORPHA:432Normosmic congenital hypogonadotropic hypogonadism34
HP:0030347HP:0030347Abnormal circulating androgen level0TERT CL E G H701511730ORPHA:1501Adrenocortical carcinoma238
HP:0030347HP:0030347Abnormal circulating androgen level0TERT CL E G H701511730ORPHA:2495Meningioma238
HP:0030347HP:0030347Abnormal circulating androgen level0TP53 CL E G H715711998ORPHA:1501Adrenocortical carcinoma911
HP:0030347HP:0030347Abnormal circulating androgen level0TRAF7 CL E G H8423120456ORPHA:2495Meningioma
HP:0030347HP:0030347Abnormal circulating androgen level0TXNRD2 CL E G H1058718155ORPHA:361Familial glucocorticoid deficiency85
HP:0030347HP:0030347Abnormal circulating androgen level0VAMP7 CL E G H684511486ORPHA:25151046,XY partial gonadal dysgenesis2
HP:0030347HP:0030347Abnormal circulating androgen level0WDR11 CL E G H5571713831ORPHA:432Normosmic congenital hypogonadotropic hypogonadism10
HP:0030347HP:0030347Abnormal circulating androgen level0WNT4 CL E G H5436112783ORPHA:247768Müllerian aplasia and hyperandrogenism4
HP:0030347HP:0030347Abnormal circulating androgen level0WT1 CL E G H749012796ORPHA:25151046,XY partial gonadal dysgenesis177
HP:0030347HP:0030347Abnormal circulating androgen level0WWOX CL E G H5174112799ORPHA:25151046,XY partial gonadal dysgenesis149
HP:0030347HP:0030347Abnormal circulating androgen level0ZFPM2 CL E G H2341416700ORPHA:25151046,XY partial gonadal dysgenesis31
HP:0030347HP:0030347Abnormal circulating androgen level0ZNRF3 CL E G H8413318126ORPHA:1501Adrenocortical carcinoma
HP:0030347HP:0033527Decreased gonadotropin-stimulated testosterone-to-androstenedione ratio1 CL E G H
HP:0030347HP:0030087Abnormal circulating testosterone concentration1AKT1 CL E G H207391ORPHA:2495Meningioma54
HP:0030347HP:0030349Decreased circulating androgen concentration1AKT1 CL E G H207391ORPHA:2495Meningioma54
HP:0030347HP:0030348Increased circulating androgen concentration1ALG6 CL E G H2992923157ORPHA:79320ALG6-CDGHP:0040284 - Very rare66
HP:0030347HP:0030348Increased circulating androgen concentration1ALMS1 CL E G H7840428ORPHA:64Alström syndromeHP:0040283 - Occasional404
HP:0030347HP:0030087Abnormal circulating testosterone concentration1ANOS1 CL E G H37306211OMIM:308700Hypogonadotropic hypogonadism 1 with or without anosmia65
HP:0030347HP:0030349Decreased circulating androgen concentration1ANOS1 CL E G H37306211OMIM:308700Hypogonadotropic hypogonadism 1 with or without anosmia65
HP:0030347HP:0030087Abnormal circulating testosterone concentration1AR CL E G H367644ORPHA:99429Complete androgen insensitivity syndrome125
HP:0030347HP:0030348Increased circulating androgen concentration1AR CL E G H367644ORPHA:99429Complete androgen insensitivity syndrome125
HP:0030347HP:0030087Abnormal circulating testosterone concentration1AR CL E G H367644ORPHA:90797Partial androgen insensitivity syndrome125
HP:0030347HP:0030348Increased circulating androgen concentration1AR CL E G H367644ORPHA:90797Partial androgen insensitivity syndrome125
HP:0030347HP:0030087Abnormal circulating testosterone concentration1B4GALNT1 CL E G H25834117ORPHA:101006Autosomal recessive spastic paraplegia type 2625
HP:0030347HP:0030349Decreased circulating androgen concentration1B4GALNT1 CL E G H25834117ORPHA:101006Autosomal recessive spastic paraplegia type 2625
HP:0030347HP:0030087Abnormal circulating testosterone concentration1B4GALNT1 CL E G H25834117OMIM:609195Spastic paraplegia 26, autosomal recessive25
HP:0030347HP:0030349Decreased circulating androgen concentration1B4GALNT1 CL E G H25834117OMIM:609195Spastic paraplegia 26, autosomal recessive25
HP:0030347HP:0030087Abnormal circulating testosterone concentration1BAP1 CL E G H8314950ORPHA:2495Meningioma184
HP:0030347HP:0030349Decreased circulating androgen concentration1BAP1 CL E G H8314950ORPHA:2495Meningioma184
HP:0030347HP:0030349Decreased circulating androgen concentration1BMP6 CL E G H6541073ORPHA:465508Symptomatic form of hemochromatosis type 1
HP:0030347HP:0030087Abnormal circulating testosterone concentration1BMP6 CL E G H6541073ORPHA:465508Symptomatic form of hemochromatosis type 1
HP:0030347HP:0030348Increased circulating androgen concentration1CDKN2A CL E G H10291787ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent289
HP:0030347HP:0033811Abnormal circulating androstenedione concentration1CDKN2A CL E G H10291787ORPHA:1501Adrenocortical carcinoma289
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1CDKN2A CL E G H10291787ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent289
HP:0030347HP:0030087Abnormal circulating testosterone concentration1CHD7 CL E G H5563620626ORPHA:432Normosmic congenital hypogonadotropic hypogonadism515
HP:0030347HP:0030349Decreased circulating androgen concentration1CHD7 CL E G H5563620626ORPHA:432Normosmic congenital hypogonadotropic hypogonadism515
HP:0030347HP:0030348Increased circulating androgen concentration1CLN3 CL E G H12012074ORPHA:228346CLN3 disease216
HP:0030347HP:0030087Abnormal circulating testosterone concentration1CPE CL E G H13632303OMIM:619326BDV SYNDROME; BDVS
HP:0030347HP:0030349Decreased circulating androgen concentration1CPE CL E G H13632303OMIM:619326BDV SYNDROME; BDVS
HP:0030347HP:0033811Abnormal circulating androstenedione concentration1CTNNB1 CL E G H14992514ORPHA:1501Adrenocortical carcinoma88
HP:0030347HP:0030348Increased circulating androgen concentration1CTNNB1 CL E G H14992514ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent88
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1CTNNB1 CL E G H14992514ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent88
HP:0030347HP:0030087Abnormal circulating testosterone concentration1CYB5A CL E G H15282570ORPHA:9079646,XY disorder of sex development due to isolated 17,20-lyase deficiency2
HP:0030347HP:0030349Decreased circulating androgen concentration1CYB5A CL E G H15282570ORPHA:9079646,XY disorder of sex development due to isolated 17,20-lyase deficiencyHP:0040281 - Very frequent2
HP:0030347HP:0030349Decreased circulating androgen concentration1CYP11A1 CL E G H15832590ORPHA:16855846,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiencyHP:0040281 - Very frequent31
HP:0030347HP:0030349Decreased circulating androgen concentration1CYP11A1 CL E G H15832590ORPHA:289548Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiencyHP:0040281 - Very frequent31
HP:0030347HP:0033811Abnormal circulating androstenedione concentration1CYP11B1 CL E G H15842591OMIM:202010Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency112
HP:0030347HP:0030348Increased circulating androgen concentration1CYP11B1 CL E G H15842591OMIM:202010Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency112
HP:0030347HP:0030087Abnormal circulating testosterone concentration1CYP11B1 CL E G H15842591OMIM:202010Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency112
HP:0030347HP:0030348Increased circulating androgen concentration1CYP11B1 CL E G H15842591ORPHA:90795Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiencyHP:0040281 - Very frequent112
HP:0030347HP:0033811Abnormal circulating androstenedione concentration1CYP11B1 CL E G H15842591ORPHA:90795Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency112
HP:0030347HP:0030087Abnormal circulating testosterone concentration1CYP11B1 CL E G H15842591ORPHA:90795Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency112
HP:0030347HP:0030087Abnormal circulating testosterone concentration1CYP17A1 CL E G H15862593ORPHA:9079646,XY disorder of sex development due to isolated 17,20-lyase deficiency53
HP:0030347HP:0030349Decreased circulating androgen concentration1CYP17A1 CL E G H15862593ORPHA:9079646,XY disorder of sex development due to isolated 17,20-lyase deficiencyHP:0040281 - Very frequent53
HP:0030347HP:0030349Decreased circulating androgen concentration1CYP17A1 CL E G H15862593ORPHA:90793Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency53
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1CYP17A1 CL E G H15862593ORPHA:90793Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiencyHP:0040281 - Very frequent53
HP:0030347HP:0030087Abnormal circulating testosterone concentration1CYP17A1 CL E G H15862593ORPHA:90793Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency53
HP:0030347HP:0030349Decreased circulating androgen concentration1DCAF17 CL E G H8006725784ORPHA:3464Woodhouse-Sakati syndrome87
HP:0030347HP:0030087Abnormal circulating testosterone concentration1DCAF17 CL E G H8006725784OMIM:241080Woodhouse-Sakati syndrome87
HP:0030347HP:0030087Abnormal circulating testosterone concentration1DCAF17 CL E G H8006725784ORPHA:3464Woodhouse-Sakati syndrome87
HP:0030347HP:0030349Decreased circulating androgen concentration1DCAF17 CL E G H8006725784OMIM:241080Woodhouse-Sakati syndrome87
HP:0030347HP:0030349Decreased circulating androgen concentration1DHH CL E G H508462865ORPHA:16856346,XY gonadal dysgenesis-motor and sensory neuropathy syndrome21
HP:0030347HP:0030087Abnormal circulating testosterone concentration1DHH CL E G H508462865ORPHA:16856346,XY gonadal dysgenesis-motor and sensory neuropathy syndrome21
HP:0030347HP:0030087Abnormal circulating testosterone concentration1DHX37 CL E G H5764717210OMIM:27325046, XY sex reversal 112
HP:0030347HP:0030349Decreased circulating androgen concentration1DHX37 CL E G H5764717210OMIM:27325046, XY sex reversal 112
HP:0030347HP:0030087Abnormal circulating testosterone concentration1DHX37 CL E G H5764717210ORPHA:25151046,XY partial gonadal dysgenesis2
HP:0030347HP:0030349Decreased circulating androgen concentration1DHX37 CL E G H5764717210ORPHA:25151046,XY partial gonadal dysgenesis2
HP:0030347HP:0030349Decreased circulating androgen concentration1DMRT3 CL E G H5852413909ORPHA:25151046,XY partial gonadal dysgenesis1
HP:0030347HP:0030087Abnormal circulating testosterone concentration1DMRT3 CL E G H5852413909ORPHA:25151046,XY partial gonadal dysgenesis1
HP:0030347HP:0030349Decreased circulating androgen concentration1DMXL2 CL E G H233122938ORPHA:453533Polyendocrine-polyneuropathy syndrome3
HP:0030347HP:0030087Abnormal circulating testosterone concentration1DMXL2 CL E G H233122938ORPHA:453533Polyendocrine-polyneuropathy syndrome3
HP:0030347HP:0030087Abnormal circulating testosterone concentration1DUSP6 CL E G H18483072ORPHA:432Normosmic congenital hypogonadotropic hypogonadism4
HP:0030347HP:0030349Decreased circulating androgen concentration1DUSP6 CL E G H18483072ORPHA:432Normosmic congenital hypogonadotropic hypogonadism4
HP:0030347HP:0030087Abnormal circulating testosterone concentration1FGD1 CL E G H22453663OMIM:305400Aarskog-Scott syndrome62
HP:0030347HP:0030349Decreased circulating androgen concentration1FGD1 CL E G H22453663OMIM:305400Aarskog-Scott syndrome62
HP:0030347HP:0030087Abnormal circulating testosterone concentration1FGF17 CL E G H88223673ORPHA:432Normosmic congenital hypogonadotropic hypogonadism3
HP:0030347HP:0030349Decreased circulating androgen concentration1FGF17 CL E G H88223673ORPHA:432Normosmic congenital hypogonadotropic hypogonadism3
HP:0030347HP:0030349Decreased circulating androgen concentration1FGF8 CL E G H22533686ORPHA:432Normosmic congenital hypogonadotropic hypogonadism17
HP:0030347HP:0030087Abnormal circulating testosterone concentration1FGF8 CL E G H22533686ORPHA:432Normosmic congenital hypogonadotropic hypogonadism17
HP:0030347HP:0030087Abnormal circulating testosterone concentration1FGFR1 CL E G H22603688ORPHA:432Normosmic congenital hypogonadotropic hypogonadism172
HP:0030347HP:0030349Decreased circulating androgen concentration1FGFR1 CL E G H22603688ORPHA:432Normosmic congenital hypogonadotropic hypogonadism172
HP:0030347HP:0030087Abnormal circulating testosterone concentration1FSHB CL E G H24883964ORPHA:52901Isolated follicle stimulating hormone deficiency23
HP:0030347HP:0030349Decreased circulating androgen concentration1FSHB CL E G H24883964ORPHA:52901Isolated follicle stimulating hormone deficiency23
HP:0030347HP:0030087Abnormal circulating testosterone concentration1FSHR CL E G H24923969ORPHA:64739Ovarian hyperstimulation syndrome50
HP:0030347HP:0030348Increased circulating androgen concentration1FSHR CL E G H24923969ORPHA:64739Ovarian hyperstimulation syndrome50
HP:0030347HP:0030087Abnormal circulating testosterone concentration1GATA4 CL E G H26264173ORPHA:25151046,XY partial gonadal dysgenesis87
HP:0030347HP:0030349Decreased circulating androgen concentration1GATA4 CL E G H26264173ORPHA:25151046,XY partial gonadal dysgenesis87
HP:0030347HP:0030087Abnormal circulating testosterone concentration1GCNA CL E G H9395315805OMIM:301077SPERMATOGENIC FAILURE, X-LINKED, 4; SPGFX4
HP:0030347HP:0030349Decreased circulating androgen concentration1GCNA CL E G H9395315805OMIM:301077SPERMATOGENIC FAILURE, X-LINKED, 4; SPGFX4
HP:0030347HP:0030348Increased circulating androgen concentration1GNAS CL E G H27784392ORPHA:562McCune-Albright syndrome101
HP:0030347HP:0030087Abnormal circulating testosterone concentration1GNAS CL E G H27784392ORPHA:562McCune-Albright syndrome101
HP:0030347HP:0030087Abnormal circulating testosterone concentration1GNRH1 CL E G H27964419OMIM:614841Hypogonadotropic hypogonadism 12 with or without anosmia15
HP:0030347HP:0030349Decreased circulating androgen concentration1GNRH1 CL E G H27964419OMIM:614841Hypogonadotropic hypogonadism 12 with or without anosmia15
HP:0030347HP:0030087Abnormal circulating testosterone concentration1GNRH1 CL E G H27964419ORPHA:432Normosmic congenital hypogonadotropic hypogonadism15
HP:0030347HP:0030349Decreased circulating androgen concentration1GNRH1 CL E G H27964419ORPHA:432Normosmic congenital hypogonadotropic hypogonadism15
HP:0030347HP:0030087Abnormal circulating testosterone concentration1GNRHR CL E G H27984421ORPHA:432Normosmic congenital hypogonadotropic hypogonadism92
HP:0030347HP:0030349Decreased circulating androgen concentration1GNRHR CL E G H27984421ORPHA:432Normosmic congenital hypogonadotropic hypogonadism92
HP:0030347HP:0030349Decreased circulating androgen concentration1HFE CL E G H30774886ORPHA:465508Symptomatic form of hemochromatosis type 138
HP:0030347HP:0030087Abnormal circulating testosterone concentration1HFE CL E G H30774886ORPHA:465508Symptomatic form of hemochromatosis type 138
HP:0030347HP:0030087Abnormal circulating testosterone concentration1HS6ST1 CL E G H93945201ORPHA:432Normosmic congenital hypogonadotropic hypogonadism8
HP:0030347HP:0030349Decreased circulating androgen concentration1HS6ST1 CL E G H93945201ORPHA:432Normosmic congenital hypogonadotropic hypogonadism8
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiencyHP:0040282 - Frequent34
HP:0030347HP:0033811Abnormal circulating androstenedione concentration1HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency34
HP:0030347HP:0030087Abnormal circulating testosterone concentration1HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency34
HP:0030347HP:0030349Decreased circulating androgen concentration1HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency34
HP:0030347HP:0030348Increased circulating androgen concentration1HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency34
HP:0030347HP:0030348Increased circulating androgen concentration1INSR CL E G H36436091ORPHA:769Rabson-Mendenhall syndromeHP:0040282 - Frequent229
HP:0030347HP:0030087Abnormal circulating testosterone concentration1INSR CL E G H36436091ORPHA:769Rabson-Mendenhall syndrome229
HP:0030347HP:0030087Abnormal circulating testosterone concentration1KISS1 CL E G H38146341ORPHA:432Normosmic congenital hypogonadotropic hypogonadism3
HP:0030347HP:0030349Decreased circulating androgen concentration1KISS1 CL E G H38146341ORPHA:432Normosmic congenital hypogonadotropic hypogonadism3
HP:0030347HP:0030087Abnormal circulating testosterone concentration1KISS1R CL E G H846344510ORPHA:432Normosmic congenital hypogonadotropic hypogonadism14
HP:0030347HP:0030349Decreased circulating androgen concentration1KISS1R CL E G H846344510ORPHA:432Normosmic congenital hypogonadotropic hypogonadism14
HP:0030347HP:0030087Abnormal circulating testosterone concentration1LEP CL E G H39526553ORPHA:66628Obesity due to congenital leptin deficiency47
HP:0030347HP:0030349Decreased circulating androgen concentration1LEP CL E G H39526553ORPHA:66628Obesity due to congenital leptin deficiency47
HP:0030347HP:0030349Decreased circulating androgen concentration1LEPR CL E G H39536554ORPHA:179494Obesity due to leptin receptor gene deficiency46
HP:0030347HP:0030087Abnormal circulating testosterone concentration1LEPR CL E G H39536554ORPHA:179494Obesity due to leptin receptor gene deficiency46
HP:0030347HP:0030349Decreased circulating androgen concentration1LGR4 CL E G H5536613299OMIM:619613DELAYED PUBERTY, SELF-LIMITED; DPSL1
HP:0030347HP:0030087Abnormal circulating testosterone concentration1LGR4 CL E G H5536613299OMIM:619613DELAYED PUBERTY, SELF-LIMITED; DPSL1
HP:0030347HP:0030087Abnormal circulating testosterone concentration1LHB CL E G H39726584OMIM:228300Hypogonadotropic hypogonadism 23 without anosmia9
HP:0030347HP:0030349Decreased circulating androgen concentration1LHB CL E G H39726584OMIM:228300Hypogonadotropic hypogonadism 23 without anosmia9
HP:0030347HP:0030087Abnormal circulating testosterone concentration1MAP3K1 CL E G H42146848ORPHA:25151046,XY partial gonadal dysgenesis13
HP:0030347HP:0030349Decreased circulating androgen concentration1MAP3K1 CL E G H42146848ORPHA:25151046,XY partial gonadal dysgenesis13
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1MC2R CL E G H41586930ORPHA:361Familial glucocorticoid deficiency94
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1MRAP CL E G H562461304ORPHA:361Familial glucocorticoid deficiency26
HP:0030347HP:0030087Abnormal circulating testosterone concentration1NDNF CL E G H7962526256OMIM:618841HYPOGONADOTROPIC HYPOGONADISM 25 WITH ANOSMIA; HH25
HP:0030347HP:0030349Decreased circulating androgen concentration1NDNF CL E G H7962526256OMIM:618841HYPOGONADOTROPIC HYPOGONADISM 25 WITH ANOSMIA; HH25
HP:0030347HP:0030349Decreased circulating androgen concentration1NF2 CL E G H47717773ORPHA:2495Meningioma220
HP:0030347HP:0030087Abnormal circulating testosterone concentration1NF2 CL E G H47717773ORPHA:2495Meningioma220
HP:0030347HP:0030349Decreased circulating androgen concentration1NFKB2 CL E G H47917795ORPHA:293978Deficiency in anterior pituitary function-variable immunodeficiency syndromeHP:0040283 - Occasional11
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1NNT CL E G H235307863ORPHA:361Familial glucocorticoid deficiency13
HP:0030347HP:0030087Abnormal circulating testosterone concentration1NR0B1 CL E G H1907960ORPHA:25151046,XY partial gonadal dysgenesis48
HP:0030347HP:0030349Decreased circulating androgen concentration1NR0B1 CL E G H1907960ORPHA:25151046,XY partial gonadal dysgenesis48
HP:0030347HP:0030087Abnormal circulating testosterone concentration1NR2F2 CL E G H70267976OMIM:61890146,XX SEX REVERSAL 5; SRXX513
HP:0030347HP:0030348Increased circulating androgen concentration1NR2F2 CL E G H70267976OMIM:61890146,XX SEX REVERSAL 5; SRXX513
HP:0030347HP:0030087Abnormal circulating testosterone concentration1NR3C1 CL E G H29087978ORPHA:786Generalized glucocorticoid resistance syndromeHP:0040282 - Frequent79
HP:0030347HP:0030087Abnormal circulating testosterone concentration1NR5A1 CL E G H25167983ORPHA:25151046,XY partial gonadal dysgenesis38
HP:0030347HP:0030349Decreased circulating androgen concentration1NR5A1 CL E G H25167983ORPHA:25151046,XY partial gonadal dysgenesis38
HP:0030347HP:0030087Abnormal circulating testosterone concentration1NSMF CL E G H2601229843ORPHA:432Normosmic congenital hypogonadotropic hypogonadism6
HP:0030347HP:0030349Decreased circulating androgen concentration1NSMF CL E G H2601229843ORPHA:432Normosmic congenital hypogonadotropic hypogonadism6
HP:0030347HP:0030349Decreased circulating androgen concentration1PDGFB CL E G H51558800ORPHA:2495Meningioma9
HP:0030347HP:0030087Abnormal circulating testosterone concentration1PDGFB CL E G H51558800ORPHA:2495Meningioma9
HP:0030347HP:0030087Abnormal circulating testosterone concentration1PIK3CA CL E G H52908975ORPHA:2495Meningioma162
HP:0030347HP:0030349Decreased circulating androgen concentration1PIK3CA CL E G H52908975ORPHA:2495Meningioma162
HP:0030347HP:0030349Decreased circulating androgen concentration1POLA1 CL E G H54229173ORPHA:163976X-linked intellectual disability, Van Esch type2
HP:0030347HP:0030087Abnormal circulating testosterone concentration1POLA1 CL E G H54229173ORPHA:163976X-linked intellectual disability, Van Esch type2
HP:0030347HP:0030348Increased circulating androgen concentration1POLR3A CL E G H1112830074ORPHA:3455Wiedemann-Rautenstrauch syndrome138
HP:0030347HP:0030348Increased circulating androgen concentration1POLR3A CL E G H1112830074OMIM:264090Wiedemann-Rautenstrauch syndrome138
HP:0030347HP:0030087Abnormal circulating testosterone concentration1POLR3A CL E G H1112830074ORPHA:3455Wiedemann-Rautenstrauch syndrome138
HP:0030347HP:0030087Abnormal circulating testosterone concentration1POLR3A CL E G H1112830074OMIM:264090Wiedemann-Rautenstrauch syndrome138
HP:0030347HP:0031215Decreased circulating dehydroepiandrosterone-sulfate concentration1POR CL E G H54479208ORPHA:95699Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiencyHP:0040282 - Frequent76
HP:0030347HP:0030349Decreased circulating androgen concentration1POR CL E G H54479208ORPHA:95699Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiencyHP:0040283 - Occasional76
HP:0030347HP:0030348Increased circulating androgen concentration1PRKAR1A CL E G H55739388ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent134
HP:0030347HP:0033811Abnormal circulating androstenedione concentration1PRKAR1A CL E G H55739388ORPHA:1501Adrenocortical carcinoma134
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1PRKAR1A CL E G H55739388ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent134
HP:0030347HP:0030348Increased circulating androgen concentration1PRKAR1A CL E G H55739388OMIM:610489Pigmented nodular adrenocortical disease, primary, 1134
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1PRKAR1A CL E G H55739388OMIM:610489Pigmented nodular adrenocortical disease, primary, 1134
HP:0030347HP:0030087Abnormal circulating testosterone concentration1PRKAR1A CL E G H55739388OMIM:610489Pigmented nodular adrenocortical disease, primary, 1134
HP:0030347HP:0030349Decreased circulating androgen concentration1PROK2 CL E G H6067518455ORPHA:432Normosmic congenital hypogonadotropic hypogonadism9
HP:0030347HP:0030087Abnormal circulating testosterone concentration1PROK2 CL E G H6067518455ORPHA:432Normosmic congenital hypogonadotropic hypogonadism9
HP:0030347HP:0030087Abnormal circulating testosterone concentration1PROKR2 CL E G H12867415836ORPHA:432Normosmic congenital hypogonadotropic hypogonadism34
HP:0030347HP:0030349Decreased circulating androgen concentration1PROKR2 CL E G H12867415836ORPHA:432Normosmic congenital hypogonadotropic hypogonadism34
HP:0030347HP:0030087Abnormal circulating testosterone concentration1RBM28 CL E G H5513121863ORPHA:157954ANE syndrome1
HP:0030347HP:0030349Decreased circulating androgen concentration1RBM28 CL E G H5513121863ORPHA:157954ANE syndrome1
HP:0030347HP:0030349Decreased circulating androgen concentration1SEMA3A CL E G H1037110723OMIM:614897Hypogonadotropic hypogonadism 16 with or without anosmia14
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SEMA3A CL E G H1037110723OMIM:614897Hypogonadotropic hypogonadism 16 with or without anosmia14
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SLC39A4 CL E G H5563017129OMIM:201100Acrodermatitis enteropathica, Zinc-Deficiency type55
HP:0030347HP:0030349Decreased circulating androgen concentration1SLC39A4 CL E G H5563017129OMIM:201100Acrodermatitis enteropathica, Zinc-Deficiency type55
HP:0030347HP:0030349Decreased circulating androgen concentration1SMARCB1 CL E G H659811103ORPHA:2495Meningioma87
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SMARCB1 CL E G H659811103ORPHA:2495Meningioma87
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SMARCE1 CL E G H660511109ORPHA:2495Meningioma47
HP:0030347HP:0030349Decreased circulating androgen concentration1SMARCE1 CL E G H660511109ORPHA:2495Meningioma47
HP:0030347HP:0030349Decreased circulating androgen concentration1SMO CL E G H660811119ORPHA:2495Meningioma22
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SMO CL E G H660811119ORPHA:2495Meningioma22
HP:0030347HP:0030349Decreased circulating androgen concentration1SOX9 CL E G H666211204ORPHA:25151046,XY partial gonadal dysgenesis109
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SOX9 CL E G H666211204ORPHA:25151046,XY partial gonadal dysgenesis109
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SPRY4 CL E G H8184815533ORPHA:432Normosmic congenital hypogonadotropic hypogonadism5
HP:0030347HP:0030349Decreased circulating androgen concentration1SPRY4 CL E G H8184815533ORPHA:432Normosmic congenital hypogonadotropic hypogonadism5
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SRY CL E G H673611311ORPHA:177245,X/46,XY mixed gonadal dysgenesis23
HP:0030347HP:0030349Decreased circulating androgen concentration1SRY CL E G H673611311ORPHA:177245,X/46,XY mixed gonadal dysgenesis23
HP:0030347HP:0030349Decreased circulating androgen concentration1SRY CL E G H673611311ORPHA:25151046,XY partial gonadal dysgenesis23
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SRY CL E G H673611311ORPHA:25151046,XY partial gonadal dysgenesis23
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1STAR CL E G H677011359ORPHA:361Familial glucocorticoid deficiency45
HP:0030347HP:0030087Abnormal circulating testosterone concentration1SUFU CL E G H5168416466ORPHA:2495Meningioma124
HP:0030347HP:0030349Decreased circulating androgen concentration1SUFU CL E G H5168416466ORPHA:2495Meningioma124
HP:0030347HP:0030349Decreased circulating androgen concentration1TAC3 CL E G H686611521ORPHA:432Normosmic congenital hypogonadotropic hypogonadism6
HP:0030347HP:0030087Abnormal circulating testosterone concentration1TAC3 CL E G H686611521ORPHA:432Normosmic congenital hypogonadotropic hypogonadism6
HP:0030347HP:0030349Decreased circulating androgen concentration1TACR3 CL E G H687011528ORPHA:432Normosmic congenital hypogonadotropic hypogonadism34
HP:0030347HP:0030087Abnormal circulating testosterone concentration1TACR3 CL E G H687011528ORPHA:432Normosmic congenital hypogonadotropic hypogonadism34
HP:0030347HP:0030348Increased circulating androgen concentration1TERT CL E G H701511730ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent238
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1TERT CL E G H701511730ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent238
HP:0030347HP:0033811Abnormal circulating androstenedione concentration1TERT CL E G H701511730ORPHA:1501Adrenocortical carcinoma238
HP:0030347HP:0030349Decreased circulating androgen concentration1TERT CL E G H701511730ORPHA:2495Meningioma238
HP:0030347HP:0030087Abnormal circulating testosterone concentration1TERT CL E G H701511730ORPHA:2495Meningioma238
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1TP53 CL E G H715711998ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent911
HP:0030347HP:0033811Abnormal circulating androstenedione concentration1TP53 CL E G H715711998ORPHA:1501Adrenocortical carcinoma911
HP:0030347HP:0030348Increased circulating androgen concentration1TP53 CL E G H715711998ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent911
HP:0030347HP:0030087Abnormal circulating testosterone concentration1TRAF7 CL E G H8423120456ORPHA:2495Meningioma
HP:0030347HP:0030349Decreased circulating androgen concentration1TRAF7 CL E G H8423120456ORPHA:2495Meningioma
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1TXNRD2 CL E G H1058718155ORPHA:361Familial glucocorticoid deficiency85
HP:0030347HP:0030349Decreased circulating androgen concentration1VAMP7 CL E G H684511486ORPHA:25151046,XY partial gonadal dysgenesis2
HP:0030347HP:0030087Abnormal circulating testosterone concentration1VAMP7 CL E G H684511486ORPHA:25151046,XY partial gonadal dysgenesis2
HP:0030347HP:0030349Decreased circulating androgen concentration1WDR11 CL E G H5571713831ORPHA:432Normosmic congenital hypogonadotropic hypogonadism10
HP:0030347HP:0030087Abnormal circulating testosterone concentration1WDR11 CL E G H5571713831ORPHA:432Normosmic congenital hypogonadotropic hypogonadism10
HP:0030347HP:0030348Increased circulating androgen concentration1WNT4 CL E G H5436112783ORPHA:247768Müllerian aplasia and hyperandrogenism4
HP:0030347HP:0030087Abnormal circulating testosterone concentration1WNT4 CL E G H5436112783ORPHA:247768Müllerian aplasia and hyperandrogenism4
HP:0030347HP:0030349Decreased circulating androgen concentration1WT1 CL E G H749012796ORPHA:25151046,XY partial gonadal dysgenesis177
HP:0030347HP:0030087Abnormal circulating testosterone concentration1WT1 CL E G H749012796ORPHA:25151046,XY partial gonadal dysgenesis177
HP:0030347HP:0030349Decreased circulating androgen concentration1WWOX CL E G H5174112799ORPHA:25151046,XY partial gonadal dysgenesis149
HP:0030347HP:0030087Abnormal circulating testosterone concentration1WWOX CL E G H5174112799ORPHA:25151046,XY partial gonadal dysgenesis149
HP:0030347HP:0030087Abnormal circulating testosterone concentration1ZFPM2 CL E G H2341416700ORPHA:25151046,XY partial gonadal dysgenesis31
HP:0030347HP:0030349Decreased circulating androgen concentration1ZFPM2 CL E G H2341416700ORPHA:25151046,XY partial gonadal dysgenesis31
HP:0030347HP:0033811Abnormal circulating androstenedione concentration1ZNRF3 CL E G H8413318126ORPHA:1501Adrenocortical carcinoma
HP:0030347HP:0500022Abnormal circulating dehydroepiandrosterone concentration1ZNRF3 CL E G H8413318126ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent
HP:0030347HP:0030348Increased circulating androgen concentration1ZNRF3 CL E G H8413318126ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent
HP:0030347HP:0033812Decreased circulating androstenedione concentration2 CL E G H
HP:0030347HP:0040171Decreased serum testosterone concentration2AKT1 CL E G H207391ORPHA:2495MeningiomaHP:0040282 - Frequent54
HP:0030347HP:0040171Decreased serum testosterone concentration2ANOS1 CL E G H37306211OMIM:308700Hypogonadotropic hypogonadism 1 with or without anosmia65
HP:0030347HP:0030088Increased serum testosterone level2AR CL E G H367644ORPHA:99429Complete androgen insensitivity syndromeHP:0040281 - Very frequent125
HP:0030347HP:0030088Increased serum testosterone level2AR CL E G H367644ORPHA:90797Partial androgen insensitivity syndromeHP:0040281 - Very frequent125
HP:0030347HP:0040171Decreased serum testosterone concentration2B4GALNT1 CL E G H25834117ORPHA:101006Autosomal recessive spastic paraplegia type 26HP:0040284 - Very rare25
HP:0030347HP:0040171Decreased serum testosterone concentration2B4GALNT1 CL E G H25834117OMIM:609195Spastic paraplegia 26, autosomal recessiveHP:0040283 - Occasional25
HP:0030347HP:0040171Decreased serum testosterone concentration2BAP1 CL E G H8314950ORPHA:2495MeningiomaHP:0040282 - Frequent184
HP:0030347HP:0040171Decreased serum testosterone concentration2BMP6 CL E G H6541073ORPHA:465508Symptomatic form of hemochromatosis type 1HP:0040283 - Occasional
HP:0030347HP:0025380Increased circulating androstenedione concentration2CDKN2A CL E G H10291787ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent289
HP:0030347HP:0040171Decreased serum testosterone concentration2CHD7 CL E G H5563620626ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent515
HP:0030347HP:0040171Decreased serum testosterone concentration2CPE CL E G H13632303OMIM:619326BDV SYNDROME; BDVS
HP:0030347HP:0025380Increased circulating androstenedione concentration2CTNNB1 CL E G H14992514ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent88
HP:0030347HP:0040171Decreased serum testosterone concentration2CYB5A CL E G H15282570ORPHA:9079646,XY disorder of sex development due to isolated 17,20-lyase deficiencyHP:0040281 - Very frequent2
HP:0030347HP:0030088Increased serum testosterone level2CYP11B1 CL E G H15842591OMIM:202010Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency112
HP:0030347HP:0025380Increased circulating androstenedione concentration2CYP11B1 CL E G H15842591OMIM:202010Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency112
HP:0030347HP:0030088Increased serum testosterone level2CYP11B1 CL E G H15842591ORPHA:90795Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiencyHP:0040283 - Occasional112
HP:0030347HP:0025380Increased circulating androstenedione concentration2CYP11B1 CL E G H15842591ORPHA:90795Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiencyHP:0040281 - Very frequent112
HP:0030347HP:0040171Decreased serum testosterone concentration2CYP17A1 CL E G H15862593ORPHA:9079646,XY disorder of sex development due to isolated 17,20-lyase deficiencyHP:0040281 - Very frequent53
HP:0030347HP:0040171Decreased serum testosterone concentration2CYP17A1 CL E G H15862593ORPHA:90793Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiencyHP:0040281 - Very frequent53
HP:0030347HP:0040171Decreased serum testosterone concentration2DCAF17 CL E G H8006725784OMIM:241080Woodhouse-Sakati syndrome.87
HP:0030347HP:0040171Decreased serum testosterone concentration2DCAF17 CL E G H8006725784ORPHA:3464Woodhouse-Sakati syndromeHP:0040281 - Very frequent87
HP:0030347HP:0040171Decreased serum testosterone concentration2DHH CL E G H508462865ORPHA:16856346,XY gonadal dysgenesis-motor and sensory neuropathy syndromeHP:0040281 - Very frequent21
HP:0030347HP:0040171Decreased serum testosterone concentration2DHX37 CL E G H5764717210OMIM:27325046, XY sex reversal 112
HP:0030347HP:0040171Decreased serum testosterone concentration2DHX37 CL E G H5764717210ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent2
HP:0030347HP:0040171Decreased serum testosterone concentration2DMRT3 CL E G H5852413909ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent1
HP:0030347HP:0040171Decreased serum testosterone concentration2DMXL2 CL E G H233122938ORPHA:453533Polyendocrine-polyneuropathy syndromeHP:0040282 - Frequent3
HP:0030347HP:0040171Decreased serum testosterone concentration2DUSP6 CL E G H18483072ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent4
HP:0030347HP:0040171Decreased serum testosterone concentration2FGD1 CL E G H22453663OMIM:305400Aarskog-Scott syndrome62
HP:0030347HP:0040171Decreased serum testosterone concentration2FGF17 CL E G H88223673ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent3
HP:0030347HP:0040171Decreased serum testosterone concentration2FGF8 CL E G H22533686ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent17
HP:0030347HP:0040171Decreased serum testosterone concentration2FGFR1 CL E G H22603688ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent172
HP:0030347HP:0040171Decreased serum testosterone concentration2FSHB CL E G H24883964ORPHA:52901Isolated follicle stimulating hormone deficiencyHP:0040281 - Very frequent23
HP:0030347HP:0030088Increased serum testosterone level2FSHR CL E G H24923969ORPHA:64739Ovarian hyperstimulation syndromeHP:0040281 - Very frequent50
HP:0030347HP:0040171Decreased serum testosterone concentration2GATA4 CL E G H26264173ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent87
HP:0030347HP:0040171Decreased serum testosterone concentration2GCNA CL E G H9395315805OMIM:301077SPERMATOGENIC FAILURE, X-LINKED, 4; SPGFX4
HP:0030347HP:0030088Increased serum testosterone level2GNAS CL E G H27784392ORPHA:562McCune-Albright syndromeHP:0040282 - Frequent101
HP:0030347HP:0040171Decreased serum testosterone concentration2GNRH1 CL E G H27964419OMIM:614841Hypogonadotropic hypogonadism 12 with or without anosmia.15
HP:0030347HP:0040171Decreased serum testosterone concentration2GNRH1 CL E G H27964419ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent15
HP:0030347HP:0040171Decreased serum testosterone concentration2GNRHR CL E G H27984421ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent92
HP:0030347HP:0040171Decreased serum testosterone concentration2HFE CL E G H30774886ORPHA:465508Symptomatic form of hemochromatosis type 1HP:0040283 - Occasional38
HP:0030347HP:0040171Decreased serum testosterone concentration2HS6ST1 CL E G H93945201ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent8
HP:0030347HP:0025380Increased circulating androstenedione concentration2HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiencyHP:0040282 - Frequent34
HP:0030347HP:0040171Decreased serum testosterone concentration2HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiencyHP:0040282 - Frequent34
HP:0030347HP:0030088Increased serum testosterone level2HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiencyHP:0040282 - Frequent34
HP:0030347HP:0030088Increased serum testosterone level2INSR CL E G H36436091ORPHA:769Rabson-Mendenhall syndromeHP:0040282 - Frequent229
HP:0030347HP:0040171Decreased serum testosterone concentration2KISS1 CL E G H38146341ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent3
HP:0030347HP:0040171Decreased serum testosterone concentration2KISS1R CL E G H846344510ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent14
HP:0030347HP:0040171Decreased serum testosterone concentration2LEP CL E G H39526553ORPHA:66628Obesity due to congenital leptin deficiencyHP:0040281 - Very frequent47
HP:0030347HP:0040171Decreased serum testosterone concentration2LEPR CL E G H39536554ORPHA:179494Obesity due to leptin receptor gene deficiencyHP:0040281 - Very frequent46
HP:0030347HP:0040171Decreased serum testosterone concentration2LGR4 CL E G H5536613299OMIM:619613DELAYED PUBERTY, SELF-LIMITED; DPSL1
HP:0030347HP:0040171Decreased serum testosterone concentration2LHB CL E G H39726584OMIM:228300Hypogonadotropic hypogonadism 23 without anosmia.9
HP:0030347HP:0033810Decreased circulating dihydrotestosterone concentration2LHB CL E G H39726584OMIM:228300Hypogonadotropic hypogonadism 23 without anosmia9
HP:0030347HP:0040171Decreased serum testosterone concentration2MAP3K1 CL E G H42146848ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent13
HP:0030347HP:0031214Decreased circulating dehydroepiandrosterone concentration2MC2R CL E G H41586930ORPHA:361Familial glucocorticoid deficiencyHP:0040281 - Very frequent94
HP:0030347HP:0031214Decreased circulating dehydroepiandrosterone concentration2MRAP CL E G H562461304ORPHA:361Familial glucocorticoid deficiencyHP:0040281 - Very frequent26
HP:0030347HP:0040171Decreased serum testosterone concentration2NDNF CL E G H7962526256OMIM:618841HYPOGONADOTROPIC HYPOGONADISM 25 WITH ANOSMIA; HH25
HP:0030347HP:0040171Decreased serum testosterone concentration2NF2 CL E G H47717773ORPHA:2495MeningiomaHP:0040282 - Frequent220
HP:0030347HP:0031214Decreased circulating dehydroepiandrosterone concentration2NNT CL E G H235307863ORPHA:361Familial glucocorticoid deficiencyHP:0040281 - Very frequent13
HP:0030347HP:0040171Decreased serum testosterone concentration2NR0B1 CL E G H1907960ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent48
HP:0030347HP:0030088Increased serum testosterone level2NR2F2 CL E G H70267976OMIM:61890146,XX SEX REVERSAL 5; SRXX513
HP:0030347HP:0040171Decreased serum testosterone concentration2NR5A1 CL E G H25167983ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent38
HP:0030347HP:0040171Decreased serum testosterone concentration2NSMF CL E G H2601229843ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent6
HP:0030347HP:0040171Decreased serum testosterone concentration2PDGFB CL E G H51558800ORPHA:2495MeningiomaHP:0040282 - Frequent9
HP:0030347HP:0040171Decreased serum testosterone concentration2PIK3CA CL E G H52908975ORPHA:2495MeningiomaHP:0040282 - Frequent162
HP:0030347HP:0040171Decreased serum testosterone concentration2POLA1 CL E G H54229173ORPHA:163976X-linked intellectual disability, Van Esch typeHP:0040282 - Frequent2
HP:0030347HP:0030088Increased serum testosterone level2POLR3A CL E G H1112830074ORPHA:3455Wiedemann-Rautenstrauch syndromeHP:0040284 - Very rare138
HP:0030347HP:0030088Increased serum testosterone level2POLR3A CL E G H1112830074OMIM:264090Wiedemann-Rautenstrauch syndrome.138
HP:0030347HP:0025380Increased circulating androstenedione concentration2PRKAR1A CL E G H55739388ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent134
HP:0030347HP:0031214Decreased circulating dehydroepiandrosterone concentration2PRKAR1A CL E G H55739388OMIM:610489Pigmented nodular adrenocortical disease, primary, 1134
HP:0030347HP:0030088Increased serum testosterone level2PRKAR1A CL E G H55739388OMIM:610489Pigmented nodular adrenocortical disease, primary, 1134
HP:0030347HP:0040171Decreased serum testosterone concentration2PROK2 CL E G H6067518455ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent9
HP:0030347HP:0040171Decreased serum testosterone concentration2PROKR2 CL E G H12867415836ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent34
HP:0030347HP:0040171Decreased serum testosterone concentration2RBM28 CL E G H5513121863ORPHA:157954ANE syndromeHP:0040282 - Frequent1
HP:0030347HP:0040171Decreased serum testosterone concentration2SEMA3A CL E G H1037110723OMIM:614897Hypogonadotropic hypogonadism 16 with or without anosmia14
HP:0030347HP:0040171Decreased serum testosterone concentration2SLC39A4 CL E G H5563017129OMIM:201100Acrodermatitis enteropathica, Zinc-Deficiency type.55
HP:0030347HP:0040171Decreased serum testosterone concentration2SMARCB1 CL E G H659811103ORPHA:2495MeningiomaHP:0040282 - Frequent87
HP:0030347HP:0040171Decreased serum testosterone concentration2SMARCE1 CL E G H660511109ORPHA:2495MeningiomaHP:0040282 - Frequent47
HP:0030347HP:0040171Decreased serum testosterone concentration2SMO CL E G H660811119ORPHA:2495MeningiomaHP:0040282 - Frequent22
HP:0030347HP:0040171Decreased serum testosterone concentration2SOX9 CL E G H666211204ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent109
HP:0030347HP:0040171Decreased serum testosterone concentration2SPRY4 CL E G H8184815533ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent5
HP:0030347HP:0040171Decreased serum testosterone concentration2SRY CL E G H673611311ORPHA:177245,X/46,XY mixed gonadal dysgenesisHP:0040283 - Occasional23
HP:0030347HP:0040171Decreased serum testosterone concentration2SRY CL E G H673611311ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent23
HP:0030347HP:0031214Decreased circulating dehydroepiandrosterone concentration2STAR CL E G H677011359ORPHA:361Familial glucocorticoid deficiencyHP:0040281 - Very frequent45
HP:0030347HP:0040171Decreased serum testosterone concentration2SUFU CL E G H5168416466ORPHA:2495MeningiomaHP:0040282 - Frequent124
HP:0030347HP:0040171Decreased serum testosterone concentration2TAC3 CL E G H686611521ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent6
HP:0030347HP:0040171Decreased serum testosterone concentration2TACR3 CL E G H687011528ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent34
HP:0030347HP:0025380Increased circulating androstenedione concentration2TERT CL E G H701511730ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent238
HP:0030347HP:0040171Decreased serum testosterone concentration2TERT CL E G H701511730ORPHA:2495MeningiomaHP:0040282 - Frequent238
HP:0030347HP:0025380Increased circulating androstenedione concentration2TP53 CL E G H715711998ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent911
HP:0030347HP:0040171Decreased serum testosterone concentration2TRAF7 CL E G H8423120456ORPHA:2495MeningiomaHP:0040282 - Frequent
HP:0030347HP:0031214Decreased circulating dehydroepiandrosterone concentration2TXNRD2 CL E G H1058718155ORPHA:361Familial glucocorticoid deficiencyHP:0040281 - Very frequent85
HP:0030347HP:0040171Decreased serum testosterone concentration2VAMP7 CL E G H684511486ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent2
HP:0030347HP:0040171Decreased serum testosterone concentration2WDR11 CL E G H5571713831ORPHA:432Normosmic congenital hypogonadotropic hypogonadismHP:0040281 - Very frequent10
HP:0030347HP:0030088Increased serum testosterone level2WNT4 CL E G H5436112783ORPHA:247768Müllerian aplasia and hyperandrogenismHP:0040281 - Very frequent4
HP:0030347HP:0040171Decreased serum testosterone concentration2WT1 CL E G H749012796ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent177
HP:0030347HP:0040171Decreased serum testosterone concentration2WWOX CL E G H5174112799ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent149
HP:0030347HP:0040171Decreased serum testosterone concentration2ZFPM2 CL E G H2341416700ORPHA:25151046,XY partial gonadal dysgenesisHP:0040281 - Very frequent31
HP:0030347HP:0025380Increased circulating androstenedione concentration2ZNRF3 CL E G H8413318126ORPHA:1501Adrenocortical carcinomaHP:0040282 - Frequent


Genes (88) :AKT1 ALG6 ALMS1 ANOS1 AR B4GALNT1 BAP1 BMP6 CDKN2A CHD7 CLN3 CPE CTNNB1 CYB5A CYP11A1 CYP11B1 CYP17A1 DCAF17 DHH DHX37 DMRT3 DMXL2 DUSP6 FGD1 FGF17 FGF8 FGFR1 FSHB FSHR GATA4 GCNA GNAS GNRH1 GNRHR HFE HS6ST1 HSD3B2 INSR KISS1 KISS1R LEP LEPR LGR4 LHB MAP3K1 MC2R MRAP NDNF NF2 NFKB2 NNT NR0B1 NR2F2 NR3C1 NR5A1 NSMF PDGFB PIK3CA POLA1 POLR3A POR PRKAR1A PROK2 PROKR2 RBM28 SEMA3A SLC39A4 SMARCB1 SMARCE1 SMO SOX9 SPRY4 SRY STAR SUFU TAC3 TACR3 TERT TP53 TRAF7 TXNRD2 VAMP7 WDR11 WNT4 WT1 WWOX ZFPM2 ZNRF3

Diseases (52) :ORPHA:2495 ORPHA:79320 ORPHA:64 OMIM:308700 ORPHA:99429 ORPHA:90797 ORPHA:101006 OMIM:609195 ORPHA:465508 ORPHA:1501 ORPHA:432 ORPHA:228346 OMIM:619326 ORPHA:90796 ORPHA:168558 ORPHA:289548 OMIM:202010 ORPHA:90795 ORPHA:90793 OMIM:241080 ORPHA:3464 ORPHA:168563 OMIM:273250 ORPHA:251510 ORPHA:453533 OMIM:305400 ORPHA:52901 ORPHA:64739 OMIM:301077 ORPHA:562 OMIM:614841 ORPHA:90791 ORPHA:769 ORPHA:66628 ORPHA:179494 OMIM:619613 OMIM:228300 ORPHA:361 OMIM:618841 ORPHA:293978 OMIM:618901 ORPHA:786 ORPHA:163976 OMIM:264090 ORPHA:3455 ORPHA:95699 OMIM:610489 ORPHA:157954 OMIM:614897 OMIM:201100 ORPHA:1772 ORPHA:247768
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.