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 hallux (HP:0001844)

Grandparent Node:
Deviation of toes (HP:0100498)

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

..Starting node
..Proximal placement of hallux (HP:0011926)

Term ID:

11926

Name:

Proximal placement of hallux

Synonym:

Proximal placement of big toe; Proximally placed halluces

Definition:

Proximal mislocalization of the big toe from its normal position.

Comments:

Reference:

HP:0011926

Genes and Diseases:

Child Nodes:

Sister Nodes:

Clinodactyly of hallux (HP:0040018)

Hallux valgus (HP:0001822)

Hallux varus (HP:0008080)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011926	HP:0011926	Proximal placement 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.