Human Phenotype Ontology 
Grandparent Node:
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Abnormal retinal morphology (HP:0000479)help
Parent Node:
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Retinal detachment (HP:0000541)help
..Starting node
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Peripheral retinal detachment (HP:0007929)help
Term ID: 7929
Name: Peripheral retinal detachment
Synonym:
Definition: Separation of the inner layers of the retina (neural retina) from the pigment epithelium occuring near the outer limit (periphery) of the retina.
Comments:
Reference: HP:0007929
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandExudative retinal detachment (HP:0012231) help
..expandRetinal nonattachment (HP:0007899) help
..expandRhegmatogenous retinal detachment (HP:0012230) help
..expandTractional retinal detachment (HP:0007917) 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:0007929HP:0007929Peripheral retinal detachment0 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.