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:
Clinodactyly (HP:0030084)

Grandparent Node:
Deviation of toes (HP:0100498)

Parent Node:
Deviation of the hallux (HP:0010051)

Parent Node:
Toe clinodactyly (HP:0001863)

..Starting node
..Clinodactyly of hallux (HP:0040018)

Term ID:

40018

Name:

Clinodactyly of hallux

Synonym:

Curvature of big toe

Definition:

Comments:

Reference:

HP:0040018

Genes and Diseases:

Child Nodes:

Sister Nodes:

Clinodactyly of the 2nd toe (HP:0005824)

Clinodactyly of the 3rd toe (HP:0008115)

Clinodactyly of the 4th toe (HP:0011918)

Clinodactyly of the 5th toe (HP:0001864)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040018	HP:0040018	Clinodactyly of hallux	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.