Human Phenotype Ontology 
Grandparent Node:
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Visual field defect (HP:0001123)help
Parent Node:
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Hemianopia (HP:0012377)help
..Starting node
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Homonymous hemianopia (HP:0030516)help
Term ID: 30516
Name: Homonymous hemianopia
Synonym: Homonymous hemianopsia
Definition:
Comments:
Reference: HP:0030516
Genes and Diseases:
 
       Child Nodes:
........expandCongruous homonymous hemianopia (HP:0030518) help

 Sister Nodes: 
..expandHeteronymous hemianopia (HP:0030517) 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:0030516HP:0030516Homonymous hemianopia0AMACR CL E G H23600451ORPHA:79095Congenital bile acid synthesis defect type 444
HP:0030516HP:0030518Congruous homonymous hemianopia1 CL E G H


Genes (1) :AMACR

Diseases (1) :ORPHA:79095
 

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