Human Phenotype Ontology

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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 hamate bone (HP:0004259)

Grandparent Node:
Large carpal bones (HP:0004237)

Parent Node:
Broad carpal bones (HP:0004242)

Parent Node:
Large hamate bone (HP:0004260)

..Starting node
..Wide hamate bone (HP:0004261)

Term ID:

4261

Name:

Wide hamate bone

Synonym:

Broad hamate bone; Wide unciform bone

Definition:

Comments:

Reference:

HP:0004261

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004261	HP:0004261	Wide hamate bone	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.