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DO Term : autosomal recessive limb-girdle muscular dystrophy type 2S [DOID:0110287] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the TRAPPC11 gene on chromosome 4q35.

synonyms:
muscular dystrophy, limb-girdle, type 2S,
OMIM:615356,
ICD10CM:G71.0,
LGMD2S,
615356,
ORDO:369840

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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