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 location of ears (HP:0000357)

Grandparent Node:
Abnormal pinna morphology (HP:0000377)

Parent Node:
Asymmetry of the ears (HP:0010722)

..Starting node
..Asymmetry of the position of the ears (HP:0040093)

Term ID:

40093

Name:

Asymmetry of the position of the ears

Synonym:

Uneven ears

Definition:

Comments:

Reference:

HP:0040093

Genes and Diseases:

Child Nodes:

Sister Nodes:

Asymmetry of the shape of the ears (HP:0040092)

Asymmetry of the size of ears (HP:0040091)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040093	HP:0040093	Asymmetry of the position of the ears	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.