Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal vitreous humor morphology (HP:0004327)

Parent Node:
Vitreoretinopathy (HP:0007773)

..Starting node
..Erosive vitreoretinopathy (HP:0030673)

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:

Degenerative vitreoretinopathy (HP:0007964)

Exudative vitreoretinopathy (HP:0030490)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030673	HP:0030673	Erosive vitreoretinopathy	0	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.

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