DO_rare_slim autosomal recessive limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2Y disease_ontology DOID:0110289 ORDO:424261 MIM:617072 An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the TOR1AIP1 gene on chromosome 1q24. ICD10CM:G71.0 LGMD2Y autosomal recessive muscular dystrophy due to LAP1B deficiency autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency muscular dystrophy with progressive weakness, distal contractures and rigid spine muscular dystrophy, limb-girdle, type 2Y