Human Phenotype Ontology 
Grandparent Node:
expandAbnormal retinal morphology (HP:0000479)help
Parent Node:
expandAbnormal macular morphology (HP:0001103)help
..Starting node
..expandVitreomacular adhesion (HP:0031150)help
Term ID: 31150
Name: Vitreomacular adhesion
Synonym: VMA
Definition: Perifoveal vitreous separation with remaining vitreomacular attachment and unperturbed foveal morphologic features. It is an OCT finding that is almost always the result of normal vitreous aging, which may lead to pathologic conditions.
Comments:
Reference: HP:0031150
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal foveal morphology (HP:0000493) help
..expandAbnormality morphology of the macular vasculature (HP:0030495) help
..expandAbnormality of macular pigmentation (HP:0008002) help
..expandAplasia/Hypoplasia of the macula (HP:0008059) help
..expandChoroidal neovascularization (HP:0011506) help
..expandMacular coloboma (HP:0001116) help
..expandMacular degeneration (HP:0000608) help
..expandMacular dystrophy (HP:0007754) help
..expandMacular hemorrhage (HP:0025574) help
..expandMacular hole (HP:0011508) help
..expandMacular thickening (HP:0030498) help
..expandVitreomacular traction (HP:0031151) help
..expandYellow/white lesions of the macula (HP:0030500) 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:0031150HP:0031150Vitreomacular adhesion0 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.