WormBase Tree Display for DO_term: DOID:0110296
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DOID:0110296 | Name | autosomal recessive limb-girdle muscular dystrophy type 2M | |||
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Status | Valid | ||||
Definition | An 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. | ||||
Synonym | Exact | LGMD2M | |||
MDDGC4 | |||||
muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4 | |||||
Parent | Is_a | DOID:0110274 | |||
DB_info | Database | OMIM | disease | 611588 | |
Attribute_of | Gene_by_orthology | WBGene00011554 | |||
WBGene00020307 | |||||
WBGene00020924 | |||||
WBGene00020927 | |||||
WBGene00021249 |