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DO Term : autosomal dominant limb-girdle muscular dystrophy type 1 [DOID:0110305] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the DNAJB6 gene on chromosome 7q36.

synonyms:
LGMD1D,
OMIM:603511,
autosomal dominant limb-girdle muscular dystrophy type 1E,
ICD10CM:G71.0,
ORDO:34517,
muscular dystrophy limb-girdle type 1D,
muscular dystrophy limb-girdle type 1E,
603511

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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