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 antihelix morphology (HP:0009738)

Parent Node:
Abnormality of inferior crus of antihelix (HP:0011243)

..Starting node
..Underdeveloped inferior crus of antihelix (HP:0011239)

Term ID:

11239

Name:

Underdeveloped inferior crus of antihelix

Synonym:

Antihelix, inferior crus, underdeveloped; Hypoplastic inferior crus of antihelix; Hypotrophic inferior crus of antihelix

Definition:

Decreased protrusion of the inferior crus relative to the prominence of the antihelix stem.

Comments:

Reference:

HP:0011239

Genes and Diseases:

Child Nodes:

Sister Nodes:

Broad inferior crus of antihelix (HP:0011237)

Prominent inferior crus of antihelix (HP:0011238)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011239	HP:0011239	Underdeveloped inferior crus of antihelix	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.