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:
Aplasia/Hypoplasia of the eyelid (HP:0011226)

Parent Node:
Hypoplasia of eyelid (HP:0430009)

..Starting node
..Hypoplasia of the upper eyelids (HP:0040032)

Term ID:

40032

Name:

Hypoplasia of the upper eyelids

Synonym:

Decreased size of upper eyelid; Hypotrophic upper eyelid; Short upper eyelid; Small upper eyelid; Underdevelopment of upper eyelid

Definition:

Comments:

Reference:

HP:0040032

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hypoplasia of the lower eyelids (HP:0007697)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040032	HP:0040032	Hypoplasia of the upper eyelids	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.