Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 nail (HP:0001597)

Parent Node:
Nail dystrophy (HP:0008404)

..Starting node
..Central nail canal (HP:0030818)

Term ID:

30818

Name:

Central nail canal

Synonym:

Median nail dystrophy

Definition:

The presence of a depressed line ("canal") in the center of the nail.

Comments:

Reference:

HP:0030818

Genes and Diseases:

Child Nodes:

Sister Nodes:

Dystrophic fingernails (HP:0008391)

Dystrophic toenail (HP:0001810)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030818	HP:0030818	Central nail canal	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.