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DO Term : autosomal recessive limb-girdle muscular dystrophy type 2L [DOID:0110284] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ANO5 gene on chromosome 11p14.

synonyms:
muscular dystrophy, limb-girdle, type 2L,
ICD10CM:G71.0,
OMIM:611307,
ORDO:206549,
611307,
LGMD2L

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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