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 phalanges of the 3rd toe (HP:0010330)

Grandparent Node:
Triangular shaped phalanges of the toes (HP:0010180)

Parent Node:
Metatarsal synostosis (HP:0001440)

Parent Node:
Symphalangism affecting the proximal phalanx of the 4th toe (HP:0100474)

Parent Node:
Triangular shaped phalanges of the 3rd toe (HP:0010366)

..Starting node
..Symphalangism of the proximal phalanx of the 4th toe with the 4th metatarsal (HP:0100485)

Term ID:

100485

Name:

Symphalangism of the proximal phalanx of the 4th toe with the 4th metatarsal

Synonym:

Fused innermost bone of the 4th toe with 4th long bone of foot

Definition:

Comments:

Reference:

HP:0100485

Genes and Diseases:

Child Nodes:

Sister Nodes:

Proximal/middle symphalangism of 2nd toe (HP:0100489)

Proximal/middle symphalangism of 5th toe (HP:0100482)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100485	HP:0100485	Symphalangism of the proximal phalanx of the 4th toe with the 4th metatarsal	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.