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:
Abnormality of the nose (HP:0000366)

Parent Node:
Abnormal nostril morphology (HP:0005288)

..Starting node
..Supernumerary naris (HP:0009934)

Term ID:

9934

Name:

Supernumerary naris

Synonym:

Accessory nares; Accessory nostril; Extra nostril; Supernumerary nares; Supernumerary nostrils

Definition:

The presence of more than two nostrils.

Comments:

Reference:

HP:0009934

Genes and Diseases:

Child Nodes:

Sister Nodes:

Absent nares (HP:0100596)

Anteverted nares (HP:0000463)

Asymmetry of the nares (HP:0009930)

Enlarged naris (HP:0009931)

Narrow naris (HP:0009933)

Single naris (HP:0009932)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009934	HP:0009934	Supernumerary naris	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.