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:
Radial deviation of the hand or of fingers of the hand (HP:0009485)

Parent Node:
Deviation of the thumb (HP:0009603)

Parent Node:
Radial deviation of finger (HP:0009466)

..Starting node
..obsolete Radial deviation of the thumb (HP:0040021)

Term ID:

40021

Name:

obsolete Radial deviation of the thumb

Synonym:

Definition:

Comments:

Reference:

HP:0040021

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hitchhiker thumb (HP:0001234)

Radial deviation of the 2nd finger (HP:0009467)

Radial deviation of the 3rd finger (HP:0009462)

Radial deviation of the 4th finger (HP:0009279)

Radial deviation of the 5th finger (HP:0040020)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040021	HP:0040021	obsolete Radial deviation of the 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.