Human Phenotype Ontology 
Grandparent Node:
expandAbnormal posterior eye segment morphology (HP:0004329)help
Parent Node:
expandAbnormal vitreous humor morphology (HP:0004327)help
..Starting node
..expandMembranous vitreous appearance (HP:0031153)help
Term ID: 31153
Name: Membranous vitreous appearance
Synonym: Membranous anomaly; Membranous vitreous; Membranous vitreous phenotype
Definition: Vitreous humor of the eye displaying consisting of a vestigial gel in the retrolental space bounded by a convoluted membrane.
Comments:
Reference: HP:0031153
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAmyloid deposition in the vitreous humor (HP:0007841) help
..expandAsteroid hyalosis (HP:0030672) help
..expandBeaded vitreous appearance (HP:0031154) help
..expandOptically empty vitreous (HP:0030663) help
..expandPeripheral vitreous opacities (HP:0007710) help
..expandPosterior vitreous detachment (HP:0001489) help
..expandRemnants of the hyaloid vascular system (HP:0007968) help
..expandVitreoretinopathy (HP:0007773) help
..expandVitreous floaters (HP:0100832) help
..expandVitreous hemorrhage (HP:0007902) help
..expandVitritis (HP:0011531) 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:0031153HP:0031153Membranous vitreous appearance0COL2A1 CL E G H12802200OMIM:108300Stickler syndrome, type I284


Genes (1) :COL2A1

Diseases (1) :OMIM:108300
 

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