Human Phenotype Ontology 
Grandparent Node:
Abnormal vitreous humor morphology (HP:0004327)help
Parent Node:
Vitreoretinopathy (HP:0007773)help
..Starting node
Erosive vitreoretinopathy (HP:0030673)help
Term ID: 30673
Name: Erosive vitreoretinopathy
Definition: A form of vitreoretinopathy characterized by thinning (erosion) of the retinal pigment epithelium that permits increased visualization of the choroidal vessels.
Reference: HP:0030673
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandDegenerative vitreoretinopathy (HP:0007964) help
..expandExudative vitreoretinopathy (HP:0030490) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030673HP:0030673Erosive vitreoretinopathy0 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 June 2019 release.