Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal retinal morphology (HP:0000479)help
Parent Node:
expand
Retinal detachment (HP:0000541)help
..Starting node
..expand
Retinal nonattachment (HP:0007899)help
Term ID: 7899
Name: Retinal nonattachment
Synonym: Congenital retinal non-attachment
Definition: Failure of attachment of the retina during development.
Comments:
Reference: HP:0007899
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandExudative retinal detachment (HP:0012231) help
..expandPeripheral retinal detachment (HP:0007929) 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:0007899HP:0007899Retinal nonattachment0AKT1 CL E G H207391ORPHA:744Proteus syndromeHP:0040283 - Occasional54
HP:0007899HP:0007899Retinal nonattachment0ATOH7 CL E G H22020213907OMIM:221900Persistent hyperplastic primary vitreous, autosomal recessive.HP:0003577 - Congenital onset4
HP:0007899HP:0007899Retinal nonattachment0BEST1 CL E G H743912703ORPHA:99000Adult-onset foveomacular vitelliform dystrophyHP:0040283 - Occasional182
HP:0007899HP:0007899Retinal nonattachment0IMPG1 CL E G H36176055ORPHA:99000Adult-onset foveomacular vitelliform dystrophyHP:0040283 - Occasional4
HP:0007899HP:0007899Retinal nonattachment0IMPG2 CL E G H5093918362ORPHA:99000Adult-onset foveomacular vitelliform dystrophyHP:0040283 - Occasional120
HP:0007899HP:0007899Retinal nonattachment0PRPH2 CL E G H59619942ORPHA:99000Adult-onset foveomacular vitelliform dystrophyHP:0040283 - Occasional159
HP:0007899HP:0007899Retinal nonattachment0PTEN CL E G H57289588ORPHA:744Proteus syndromeHP:0040283 - Occasional948


Genes (7) :AKT1 ATOH7 BEST1 IMPG1 IMPG2 PRPH2 PTEN

Diseases (3) :ORPHA:744 OMIM:221900 ORPHA:99000
 

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