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:
Aplasia/Hypoplasia involving the metacarpal bones (HP:0005914)

Parent Node:
Short metacarpal (HP:0010049)

..Starting node
..Cuboidal metacarpal (HP:0006011)

Term ID:

6011

Name:

Cuboidal metacarpal

Synonym:

Short, cube shaped long bone of hand

Definition:

Severely shortened metacarpal with a cuboidal appearance.

Comments:

Reference:

HP:0006011

Genes and Diseases:

Child Nodes:

Sister Nodes:

Short 1st metacarpal (HP:0010034)

Short 2nd metacarpal (HP:0010038)

Short 3rd metacarpal (HP:0010041)

Short 4th metacarpal (HP:0010044)

Short 5th metacarpal (HP:0010047)

Short metacarpals with rounded proximal ends (HP:0006161)

Shortening of all metacarpals (HP:0005720)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006011	HP:0006011	Cuboidal metacarpal	0	GDF5 CL E G H	8200	4220	OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type	.	52
HP:0006011	HP:0006011	Cuboidal metacarpal	0	GDF5 CL E G H	8200	4220	ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type	HP:0040282 - Frequent	52

Genes (1) :GDF5

Diseases (2) :OMIM:201250 ORPHA:968

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.