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)

..Starting node
..Congenital curved nail of fourth toe (HP:0008393)

Term ID:

8393

Name:

Congenital curved nail of fourth toe

Synonym:

Definition:

Comments:

Reference:

HP:0008393

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplastic/hypoplastic toenail (HP:0010624)

Dystrophic toenail (HP:0001810)

Malalignment of the great toenail (HP:0031282)

Thin toenail (HP:0012746)

Toenail dysplasia (HP:0100797)

Toenail onycholysis (HP:0040040)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008393	HP:0008393	Congenital curved nail of fourth toe	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.