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:
Retinopathy of prematurity (HP:0500049)

Parent Node:
Retinopathy of prematurity stage 5 (HP:0500056)

..Starting node
..Retinopathy of prematurity stage 5a (HP:0500057)

Term ID:

500057

Name:

Retinopathy of prematurity stage 5a

Synonym:

ROP stage 5a

Definition:

An open funnel detachment of the retina with generally traction in all four quadrants.

Comments:

Reference:

HP:0500057

Genes and Diseases:

Child Nodes:

Sister Nodes:

Retinopathy of prematurity stage 5b (HP:0500058)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500057	HP:0500057	Retinopathy of prematurity stage 5a	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.