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:
Deviation of finger (HP:0004097)

Grandparent Node:
Ulnar deviation of the hand or of fingers of the hand (HP:0001193)

Parent Node:
Ulnar deviation of finger (HP:0009465)

..Starting node
..Ulnar deviation of thumb (HP:0006156)

Term ID:

6156

Name:

Ulnar deviation of thumb

Synonym:

Curved thumb deviated towards palm; Ulnar deviation of the 1st finger

Definition:

Bending or curvature of a thumb towards the ulnar side (towards the ring finger).

Comments:

Reference:

HP:0006156

Genes and Diseases:

Child Nodes:

Sister Nodes:

Ulnar deviation of the 2nd finger (HP:0009464)

Ulnar deviation of the 3rd finger (HP:0009463)

Ulnar deviation of the 4th finger (HP:0009278)

Ulnar deviation of the 5th finger (HP:0009180)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006156	HP:0006156	Ulnar deviation of thumb	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.