Human Phenotype Ontology 
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Hemiretinal vein occlusion (HP:0020167)help
Term ID: 20167
Name: Hemiretinal vein occlusion
Synonym:
Definition: A variant of central retinal vein occlusions that involves the superior or inferior half of the retina.
Comments:
Reference: HP:0020167
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0020167HP:0020167Hemiretinal vein occlusion0 CL E G H


Genes (0) :

Diseases (0) :
 

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