Human Phenotype Ontology 
Grandparent Node:
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Abnormal retinal morphology (HP:0000479)help
Parent Node:
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Abnormal macular morphology (HP:0001103)help
..Starting node
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Vitreomacular traction (HP:0031151)help
Term ID: 31151
Name: Vitreomacular traction
Synonym: VMT
Definition: Vitreomacular traction is characterized by anomalous posterior vitreous detachment accompanied by anatomic distortion of the fovea, which may include pseudocysts, macular schisis, cystoid macular edema, and subretinal fluid. Vitreomacular traction can be subclassified by the diameter of vitreous attachment to the macular surface as measured by OCT, with attachment of 1500 micrometers or less defined as focal and attachment of more than 1500 micrometers as broad.
Comments:
Reference: HP:0031151
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 adhesion (HP:0031150) 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:0031151HP:0031151Vitreomacular traction0 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.