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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: 46, XX Disorders of Sex Development (D058489)
Parent Node: Adrenogenital Syndrome (D047808)
..Starting node ..Hyperandrogenism (D017588)
Child Nodes:
........HAIR-AN syndrome (C537629)
........Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency (C565977)
........Mullerian Aplasia and Hyperandrogenism (C567186)
Sister Nodes:
..Adrenal Hyperplasia, Congenital (D000312) 12
..Hyperandrogenism (D017588) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5336
Name:	Hyperandrogenism
Definition:	A condition caused by the excessive secretion of ANDROGENS from the ADRENAL CORTEX; the OVARIES; or the TESTES. The clinical significance in males is negligible. In women, the common manifestations are HIRSUTISM and VIRILISM as seen in patients with POLYCYSTIC OVARY SYNDROME and ADRENOCORTICAL HYPERFUNCTION.
Alternative IDs:
ParentIDs:	MESH:D047808\|MESH:D058489
TreeNumbers:	C12.706.316.064.500 \|C12.706.316.129.750 \|C13.351.875.253.064.500 \|C13.351.875.253.129.750 \|C16.131.939.316.064.500 \|C16.131.939.316.129.750 \|C19.391.119.064.500 \|C19.391.119.129.750
Synonyms:
Slim Mappings:	Congenital abnormality\|Endocrine system disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D017588 MeSH: D017588 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants