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 toe (HP:0001780)

Parent Node:
Deviation of toes (HP:0100498)

..Starting node
..Fibular deviation of toes (HP:0100500)

Term ID:

100500

Name:

Fibular deviation of toes

Synonym:

Lateral deviation of toes

Definition:

Comments:

Reference:

HP:0100500

Genes and Diseases:

Child Nodes:

Sister Nodes:

Deviation of the 2nd toe (HP:0010326)

Deviation of the 3rd toe (HP:0010332)

Deviation of the 4th toe (HP:0010338)

Deviation of the 5th toe (HP:0010344)

Deviation of the hallux (HP:0010051)

Tibial deviation of toes (HP:0100499)

Toe clinodactyly (HP:0001863)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100500	HP:0100500	Fibular deviation of toes	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.