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 external nose morphology (HP:0010938)

Parent Node:
Abnormal columella morphology (HP:0009929)

..Starting node
..High insertion of columella (HP:0012807)

Term ID:

12807

Name:

High insertion of columella

Synonym:

Ala lower than columella; Columella, high insertion

Definition:

Insertion of the posterior columella superior to the nasal base.

Comments:

Reference:

HP:0012807

Genes and Diseases:

Child Nodes:

Sister Nodes:

Broad columella (HP:0010761)

Low hanging columella (HP:0009765)

Low insertion of columella (HP:0010763)

Short columella (HP:0002000)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012807	HP:0012807	High insertion of columella	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.