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 antitragus morphology (HP:0009896)

..Starting node
..Absent antitragus (HP:0011249)

Term ID:

11249

Name:

Absent antitragus

Synonym:

Definition:

Absence of the anterosuperior prominence of the area between the bottom of the incisura and the inner margin of the antihelix.

Comments:

Reference:

HP:0011249

Genes and Diseases:

Child Nodes:

Sister Nodes:

Bifid antitragus (HP:0011250)

Everted antitragus (HP:0011248)

Prominent antitragus (HP:0008593)

Underdeveloped antitragus (HP:0011251)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011249	HP:0011249	Absent antitragus	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.