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:
Abnormal morphology of the proximal phalanx of the 3rd toe (HP:0010370)

Grandparent Node:
Duplication of phalanx of the 3rd toe (HP:0010367)

Grandparent Node:
Duplication of proximal phalanx of toe (HP:0010211)

Parent Node:
Duplication of the proximal phalanx of the 3rd toe (HP:0100404)

..Starting node
..Complete duplication of the proximal phalanx of the 3rd toe (HP:0100413)

Term ID:

100413

Name:

Complete duplication of the proximal phalanx of the 3rd toe

Synonym:

Complete duplication of the innermost 3rd toe bone

Definition:

Complete duplication of proximal phalanx of third toe.

Comments:

Reference:

HP:0100413

Genes and Diseases:

Child Nodes:

Sister Nodes:

Partial duplication of the proximal phalanx of the 3rd toe (HP:0100422)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100413	HP:0100413	Complete duplication of the proximal phalanx of the 3rd 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.