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:
Nail dysplasia (HP:0002164)

Parent Node:
Hyperconvex nail (HP:0001795)

..Starting node
..Hyperconvex toenail (HP:0030055)

Term ID:

30055

Name:

Hyperconvex toenail

Synonym:

Definition:

When viewed on end (with the tip of the toe pointing toward the examiner's eye) the curve of the toenail forms a tighter curve of convexity.

Comments:

Reference:

HP:0030055

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hyperconvex fingernails (HP:0001812)

Hyperconvex thumb nails (HP:0008407)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030055	HP:0030055	Hyperconvex toenail	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.