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DO Term : autosomal recessive limb-girdle muscular dystrophy type 2P [DOID:0110293] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding alpha-dystroglycan (DAG1) on chromosome 3p21.

synonyms:
LGMD2P,
muscular dystrophy-dystroglycanopathy (limb-girdle) type C9,
muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related,
ICD10CM:G71.0,
MDDGC9,
613818,
ORDO:280333,
OMIM:613818

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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