Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Abnormality iris morphology (HP:0000525)

Grandparent Node:
Abnormality of the vasculature of the eye (HP:0008047)

Parent Node:
Abnormal iris vasculature (HP:0007905)

..Starting node
..Iris neovascularization (HP:0011497)

Term ID:

11497

Name:

Iris neovascularization

Synonym:

Neovascularization of the iris; New blood vessel formation in iris

Definition:

New growth of vessels on the surface of the iris.

Comments:

Reference:

HP:0011497

Genes and Diseases:

Child Nodes:

Sister Nodes:

Iris hypoperfusion (HP:0012635)

Rubeosis iridis (HP:0025319)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011497	HP:0011497	Iris neovascularization	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.