Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of vision (HP:0000504)help
Parent Node:
expand
Visual field defect (HP:0001123)help
..Starting node
..expand
Hemianopia (HP:0012377)help
Term ID: 12377
Name: Hemianopia
Synonym: Hemianopsia
Definition: Partial or complete loss of vision in one half of the visual field of one or both eyes.
Comments:
Reference: HP:0012377
Genes and Diseases:
 
       Child Nodes:
........expandHomonymous hemianopia (HP:0030516) help
................... HP:0030518 Congruous homonymous hemianopia
........expandHeteronymous hemianopia (HP:0030517) help
................... HP:0030519 Congruous heteronymous hemianopia
................... HP:0030520 Binasal hemianopia
................... HP:0030521 Bitemporal hemianopia

 Sister Nodes: 
..expandAbnormal visual field test (HP:0030588) help
..expandAltitudinal visual field defect (HP:0030531) help
..expandBlind-spot enlargment (HP:0030644) help
..expandConstriction of peripheral visual field (HP:0001133) help
..expandGlaucomatous visual field defect (HP:0007854) help
..expandLarge central visual field defect (HP:0001129) help
..expandProgressive visual field defects (HP:0007987) help
..expandScotoma (HP:0000575) 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:0012377HP:0012377Hemianopia0AARS1 CL E G H1620OMIM:619661LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 2; HDLS2
HP:0012377HP:0012377Hemianopia0ADGRV1 CL E G H8405917416ORPHA:231178Usher syndrome type 2HP:0040281 - Very frequent530
HP:0012377HP:0012377Hemianopia0AIP CL E G H9049358ORPHA:2965ProlactinomaHP:0040283 - Occasional95
HP:0012377HP:0012377Hemianopia0AKT1 CL E G H207391ORPHA:2495Meningioma54
HP:0012377HP:0012377Hemianopia0AKT3 CL E G H10000393ORPHA:99802HemimegalencephalyHP:0040283 - Occasional19
HP:0012377HP:0012377Hemianopia0AMACR CL E G H23600451ORPHA:79095Congenital bile acid synthesis defect type 444
HP:0012377HP:0012377Hemianopia0ARSG CL E G H2290124102ORPHA:231183Usher syndrome type 3HP:0040281 - Very frequent
HP:0012377HP:0012377Hemianopia0BAP1 CL E G H8314950ORPHA:2495Meningioma184
HP:0012377HP:0012377Hemianopia0BRAF CL E G H6731097ORPHA:54595Craniopharyngioma276
HP:0012377HP:0012377Hemianopia0CDH23 CL E G H6407213733ORPHA:2965ProlactinomaHP:0040283 - Occasional636
HP:0012377HP:0012377Hemianopia0CDH23 CL E G H6407213733ORPHA:91347TSH-secreting pituitary adenomaHP:0040283 - Occasional636
HP:0012377HP:0012377Hemianopia0CDH23 CL E G H6407213733ORPHA:231169Usher syndrome type 1HP:0040281 - Very frequent636
HP:0012377HP:0012377Hemianopia0CEP78 CL E G H8413125740ORPHA:231183Usher syndrome type 3HP:0040281 - Very frequent9
HP:0012377HP:0012377Hemianopia0CIB2 CL E G H1051824579ORPHA:231169Usher syndrome type 1HP:0040281 - Very frequent15
HP:0012377HP:0012377Hemianopia0CLRN1 CL E G H740112605ORPHA:231183Usher syndrome type 3HP:0040281 - Very frequent60
HP:0012377HP:0012377Hemianopia0COX1 CL E G H45127419OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0COX2 CL E G H45137421OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0COX3 CL E G H45147422OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0CTNNB1 CL E G H14992514ORPHA:54595Craniopharyngioma88
HP:0012377HP:0012377Hemianopia0CYTB CL E G H45197427OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0ESPN CL E G H8371513281ORPHA:231169Usher syndrome type 1HP:0040281 - Very frequent33
HP:0012377HP:0012377Hemianopia0GNAQ CL E G H27764390ORPHA:3205Sturge-Weber syndromeHP:0040283 - Occasional7
HP:0012377HP:0012377Hemianopia0GPR101 CL E G H8355014963OMIM:300942Chromosome Xq26.3 duplication syndrome5
HP:0012377HP:0012377Hemianopia0HARS1 CL E G H30354816ORPHA:231183Usher syndrome type 3HP:0040281 - Very frequent
HP:0012377HP:0012377Hemianopia0MEN1 CL E G H42217010ORPHA:2965ProlactinomaHP:0040283 - Occasional462
HP:0012377HP:0012377Hemianopia0MTOR CL E G H24753942ORPHA:99802HemimegalencephalyHP:0040283 - Occasional68
HP:0012377HP:0012377Hemianopia0MYO7A CL E G H46477606ORPHA:231169Usher syndrome type 1HP:0040281 - Very frequent516
HP:0012377HP:0012377Hemianopia0MYO7A CL E G H46477606ORPHA:231178Usher syndrome type 2HP:0040281 - Very frequent516
HP:0012377HP:0012377Hemianopia0ND1 CL E G H45357455OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0ND5 CL E G H45407461OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0ND6 CL E G H45417462OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0NF2 CL E G H47717773ORPHA:2495Meningioma220
HP:0012377HP:0012377Hemianopia0PCDH15 CL E G H6521714674ORPHA:231169Usher syndrome type 1HP:0040281 - Very frequent352
HP:0012377HP:0012377Hemianopia0PDGFB CL E G H51558800ORPHA:2495Meningioma9
HP:0012377HP:0012377Hemianopia0PDZD7 CL E G H7995526257ORPHA:231178Usher syndrome type 2HP:0040281 - Very frequent40
HP:0012377HP:0012377Hemianopia0PIK3CA CL E G H52908975ORPHA:99802HemimegalencephalyHP:0040283 - Occasional162
HP:0012377HP:0012377Hemianopia0PIK3CA CL E G H52908975ORPHA:2495Meningioma162
HP:0012377HP:0012377Hemianopia0PRORP CL E G H969219958OMIM:619737COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 54; COXPD54
HP:0012377HP:0012377Hemianopia0SETD5 CL E G H5520925566ORPHA:404440Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiencyHP:0040283 - Occasional43
HP:0012377HP:0012377Hemianopia0SMARCB1 CL E G H659811103ORPHA:2495Meningioma87
HP:0012377HP:0012377Hemianopia0SMARCE1 CL E G H660511109ORPHA:2495Meningioma47
HP:0012377HP:0012377Hemianopia0SMO CL E G H660811119ORPHA:2495Meningioma22
HP:0012377HP:0012377Hemianopia0SUFU CL E G H5168416466ORPHA:2495Meningioma124
HP:0012377HP:0012377Hemianopia0TERT CL E G H701511730ORPHA:2495Meningioma238
HP:0012377HP:0012377Hemianopia0TRAF7 CL E G H8423120456ORPHA:2495Meningioma
HP:0012377HP:0012377Hemianopia0TREX1 CL E G H1127712269ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsHP:0040283 - Occasional56
HP:0012377HP:0012377Hemianopia0TRNC CL E G H45117477OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0TRNF CL E G H45587481OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0TRNK CL E G H45667489OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0TRNL1 CL E G H45677490OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0TRNQ CL E G H45727495OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0TRNS1 CL E G H45747497OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0TRNS2 CL E G H45757498OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0TRNS2 CL E G H45757498ORPHA:231183Usher syndrome type 3HP:0040281 - Very frequent
HP:0012377HP:0012377Hemianopia0TRNV CL E G H45777500OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0TRNW CL E G H45787501OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0012377HP:0012377Hemianopia0TUBB2B CL E G H34773330829ORPHA:300573Polymicrogyria due to TUBB2B mutationHP:0040283 - Occasional39
HP:0012377HP:0012377Hemianopia0USH1C CL E G H1008312597ORPHA:231169Usher syndrome type 1HP:0040281 - Very frequent173
HP:0012377HP:0012377Hemianopia0USH1G CL E G H12459016356ORPHA:231169Usher syndrome type 1HP:0040281 - Very frequent78
HP:0012377HP:0012377Hemianopia0USH2A CL E G H739912601ORPHA:231178Usher syndrome type 2HP:0040281 - Very frequent777
HP:0012377HP:0012377Hemianopia0WHRN CL E G H2586116361ORPHA:231178Usher syndrome type 2HP:0040281 - Very frequent155
HP:0012377HP:0030517Heteronymous hemianopia1AIP CL E G H9049358ORPHA:2965ProlactinomaHP:0040283 - Occasional95
HP:0012377HP:0030517Heteronymous hemianopia1AKT1 CL E G H207391ORPHA:2495Meningioma54
HP:0012377HP:0030516Homonymous hemianopia1AMACR CL E G H23600451ORPHA:79095Congenital bile acid synthesis defect type 444
HP:0012377HP:0030517Heteronymous hemianopia1BAP1 CL E G H8314950ORPHA:2495Meningioma184
HP:0012377HP:0030517Heteronymous hemianopia1BRAF CL E G H6731097ORPHA:54595Craniopharyngioma276
HP:0012377HP:0030517Heteronymous hemianopia1CDH23 CL E G H6407213733ORPHA:2965ProlactinomaHP:0040283 - Occasional636
HP:0012377HP:0030517Heteronymous hemianopia1CDH23 CL E G H6407213733ORPHA:91347TSH-secreting pituitary adenomaHP:0040283 - Occasional636
HP:0012377HP:0030517Heteronymous hemianopia1CTNNB1 CL E G H14992514ORPHA:54595Craniopharyngioma88
HP:0012377HP:0030517Heteronymous hemianopia1MEN1 CL E G H42217010ORPHA:2965ProlactinomaHP:0040283 - Occasional462
HP:0012377HP:0030517Heteronymous hemianopia1NF2 CL E G H47717773ORPHA:2495Meningioma220
HP:0012377HP:0030517Heteronymous hemianopia1PDGFB CL E G H51558800ORPHA:2495Meningioma9
HP:0012377HP:0030517Heteronymous hemianopia1PIK3CA CL E G H52908975ORPHA:2495Meningioma162
HP:0012377HP:0030517Heteronymous hemianopia1SMARCB1 CL E G H659811103ORPHA:2495Meningioma87
HP:0012377HP:0030517Heteronymous hemianopia1SMARCE1 CL E G H660511109ORPHA:2495Meningioma47
HP:0012377HP:0030517Heteronymous hemianopia1SMO CL E G H660811119ORPHA:2495Meningioma22
HP:0012377HP:0030517Heteronymous hemianopia1SUFU CL E G H5168416466ORPHA:2495Meningioma124
HP:0012377HP:0030517Heteronymous hemianopia1TERT CL E G H701511730ORPHA:2495Meningioma238
HP:0012377HP:0030517Heteronymous hemianopia1TRAF7 CL E G H8423120456ORPHA:2495Meningioma
HP:0012377HP:0030520Binasal hemianopia2 CL E G H
HP:0012377HP:0030519Congruous heteronymous hemianopia2 CL E G H
HP:0012377HP:0030518Congruous homonymous hemianopia2 CL E G H
HP:0012377HP:0030521Bitemporal hemianopia2AIP CL E G H9049358ORPHA:2965ProlactinomaHP:0040283 - Occasional95
HP:0012377HP:0030521Bitemporal hemianopia2AKT1 CL E G H207391ORPHA:2495MeningiomaHP:0040282 - Frequent54
HP:0012377HP:0030521Bitemporal hemianopia2BAP1 CL E G H8314950ORPHA:2495MeningiomaHP:0040282 - Frequent184
HP:0012377HP:0030521Bitemporal hemianopia2BRAF CL E G H6731097ORPHA:54595CraniopharyngiomaHP:0040282 - Frequent276
HP:0012377HP:0030521Bitemporal hemianopia2CDH23 CL E G H6407213733ORPHA:2965ProlactinomaHP:0040283 - Occasional636
HP:0012377HP:0030521Bitemporal hemianopia2CDH23 CL E G H6407213733ORPHA:91347TSH-secreting pituitary adenomaHP:0040283 - Occasional636
HP:0012377HP:0030521Bitemporal hemianopia2CTNNB1 CL E G H14992514ORPHA:54595CraniopharyngiomaHP:0040282 - Frequent88
HP:0012377HP:0030521Bitemporal hemianopia2MEN1 CL E G H42217010ORPHA:2965ProlactinomaHP:0040283 - Occasional462
HP:0012377HP:0030521Bitemporal hemianopia2NF2 CL E G H47717773ORPHA:2495MeningiomaHP:0040282 - Frequent220
HP:0012377HP:0030521Bitemporal hemianopia2PDGFB CL E G H51558800ORPHA:2495MeningiomaHP:0040282 - Frequent9
HP:0012377HP:0030521Bitemporal hemianopia2PIK3CA CL E G H52908975ORPHA:2495MeningiomaHP:0040282 - Frequent162
HP:0012377HP:0030521Bitemporal hemianopia2SMARCB1 CL E G H659811103ORPHA:2495MeningiomaHP:0040282 - Frequent87
HP:0012377HP:0030521Bitemporal hemianopia2SMARCE1 CL E G H660511109ORPHA:2495MeningiomaHP:0040282 - Frequent47
HP:0012377HP:0030521Bitemporal hemianopia2SMO CL E G H660811119ORPHA:2495MeningiomaHP:0040282 - Frequent22
HP:0012377HP:0030521Bitemporal hemianopia2SUFU CL E G H5168416466ORPHA:2495MeningiomaHP:0040282 - Frequent124
HP:0012377HP:0030521Bitemporal hemianopia2TERT CL E G H701511730ORPHA:2495MeningiomaHP:0040282 - Frequent238
HP:0012377HP:0030521Bitemporal hemianopia2TRAF7 CL E G H8423120456ORPHA:2495MeningiomaHP:0040282 - Frequent


Genes (56) :AARS1 ADGRV1 AIP AKT1 AKT3 AMACR ARSG BAP1 BRAF CDH23 CEP78 CIB2 CLRN1 COX1 COX2 COX3 CTNNB1 CYTB ESPN GNAQ GPR101 HARS1 MEN1 MTOR MYO7A ND1 ND5 ND6 NF2 PCDH15 PDGFB PDZD7 PIK3CA PRORP SETD5 SMARCB1 SMARCE1 SMO SUFU TERT TRAF7 TREX1 TRNC TRNF TRNK TRNL1 TRNQ TRNS1 TRNS2 TRNV TRNW TUBB2B USH1C USH1G USH2A WHRN

Diseases (17) :OMIM:619661 ORPHA:231178 ORPHA:2965 ORPHA:2495 ORPHA:99802 ORPHA:79095 ORPHA:231183 ORPHA:54595 ORPHA:91347 ORPHA:231169 OMIM:540000 ORPHA:3205 OMIM:300942 OMIM:619737 ORPHA:404440 ORPHA:247691 ORPHA:300573
 

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