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DO Term : split hand-foot malformation 6 [DOID:0090026] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A split-hand/foot malformation that has_material_basis_in homozygous mutation in the WNT10B gene on chromosome 12q13.

synonyms:
ORDO:2440,
NCI:C75000,
SNOMEDCT_US_2023_03_01:81208006,
MESH:C574275,
SHFM6,
225300,
UMLS_CUI:C0265554,
OMIM:225300

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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