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 eyelid morphology (HP:0000492)

Parent Node:
Ectropion (HP:0000656)

..Starting node
..Paralytic ectropion (HP:0500069)

Term ID:

500069

Name:

Paralytic ectropion

Synonym:

Definition:

A type of ectropion associated with orbicularis muscle weakness caused by cranial nerve VII palsy.

Comments:

Reference:

HP:0500069

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cicatricial ectropion (HP:0025608)

Ectropion of lower eyelids (HP:0007651)

Eversion of lateral third of lower eyelids (HP:0007655)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500069	HP:0500069	Paralytic ectropion	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.