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DO Term : muscular dystrophy-dystroglycanopathy type B14 [DOID:0112377] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A muscular dystrophy-dystroglycanopathy type B that has_material_basis_in homozygous or compound heterozygous mutation in the GMPPB gene on chromosome 3p21.31.

synonyms:
615351,
OMIM:615351,
congenital muscular dystrophy GMPPB-related,
MDDGB14

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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