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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Exudative retinal detachment (HP:0012231)help
Term ID: 12231
Name: Exudative retinal detachment
Synonym: Serous retinal detachment
Definition: A type of retinal detachment arising from damage to the outer blood-retinal barrier that allows fluid to access the subretinal space and separate the neurosensory retina from the retinal pigment epithelium.
Comments:
Reference: HP:0012231
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPeripheral retinal detachment (HP:0007929) 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:0012231HP:0012231Exudative retinal detachment0CFH CL E G H30754883ORPHA:75376Familial drusenHP:0040283 - Occasional86
HP:0012231HP:0012231Exudative retinal detachment0CFI CL E G H34265394ORPHA:75376Familial drusenHP:0040283 - Occasional57
HP:0012231HP:0012231Exudative retinal detachment0EFEMP1 CL E G H22023218ORPHA:75376Familial drusenHP:0040283 - Occasional54
HP:0012231HP:0012231Exudative retinal detachment0FRG1 CL E G H24833954OMIM:158900Facioscapulohumeral muscular dystrophy 1.1
HP:0012231HP:0012231Exudative retinal detachment0IGFBP7 CL E G H34905476OMIM:614224Retinal arterial macroaneurysm with supravalvular pulmonic stenosis.2


Genes (5) :CFH CFI EFEMP1 FRG1 IGFBP7

Diseases (3) :ORPHA:75376 OMIM:158900 OMIM:614224
 

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