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 pinna morphology (HP:0000377)

Parent Node:
Abnormal tragus morphology (HP:0009912)

..Starting node
..Bifid tragus (HP:0011269)

Term ID:

11269

Name:

Bifid tragus

Synonym:

Notched tragus; Tragus, bifid

Definition:

Increased height of the tragal ridge with a shallow indentation at the apex, giving the appearance of a double peak.

Comments:

Reference:

HP:0011269

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia/Hypoplasia of the tragus (HP:0009913)

Duplicated tragus (HP:0011270)

Prominent tragus (HP:0011271)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011269	HP:0011269	Bifid tragus	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.