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 nail (HP:0001597)

Parent Node:
Abnormal toenail morphology (HP:0008388)

Parent Node:
Onycholysis (HP:0001806)

..Starting node
..Toenail onycholysis (HP:0040040)

Term ID:

40040

Name:

Toenail onycholysis

Synonym:

Detachment of toenails; Onycholysis of toenails

Definition:

Painless and spontaneous separation of a toenail from the nail bed.

Comments:

Reference:

HP:0040040

Genes and Diseases:

Child Nodes:

Sister Nodes:

Onycholysis of fingernails (HP:0040039)

Onychomadesis (HP:0025088)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040040	HP:0040040	Toenail onycholysis	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.