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