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WormBase Tree Display for DO_term: DOID:0110296

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Name Class

DOID:0110296Nameautosomal recessive limb-girdle muscular dystrophy type 2M
StatusValid
DefinitionAn autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding fukutin (FKTN) on chromosome 9q31.
SynonymExactLGMD2M
MDDGC4
muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4
ParentIs_aDOID:0110274
DB_infoDatabaseOMIMdisease611588
Attribute_ofGene_by_orthologyWBGene00011554
WBGene00020307
WBGene00020924
WBGene00020927
WBGene00021249