Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal vitreous humor morphology (HP:0004327)help
Parent Node:
expand
Vitreoretinopathy (HP:0007773)help
..Starting node
..expand
Degenerative vitreoretinopathy (HP:0007964)help
Term ID: 7964
Name: Degenerative vitreoretinopathy
Synonym:
Definition:
Comments:
Reference: HP:0007964
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandErosive vitreoretinopathy (HP:0030673) help
..expandExudative vitreoretinopathy (HP:0030490) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007964HP:0007964Degenerative vitreoretinopathy0COL9A1 CL E G H1297614134Stickler syndrome, type 4614134C3279941OMIM17442217120210
HP:0007964HP:0007964Degenerative vitreoretinopathy0COL9A1 CL E G H1297614134Stickler syndrome, type 4614134C3279941OMIM15942217120210
HP:0007964HP:0007964Degenerative vitreoretinopathy0ERBB3 CL E G H2065607598Lethal congenital contracture syndrome 2607598C1843478OMIM1953431190151
HP:0007964HP:0007964Degenerative vitreoretinopathy0ERBB3 CL E G H2065607598Lethal congenital contracture syndrome 2607598C1843478OMIM1943431190151
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :COL9A1 ERBB3

Diseases (2) :614134 607598
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.