DO_rare_slim DO_FlyBase_slim NCIthesaurus has material basis in disease has location Kennedy's disease MIM:313200 disease_ontology MESH:D055534 UMLS_CUI:C1839259 2011-08-29T01:31:03Z NCI:C85233 A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. GARD:6818 Kennedy disease SNOMEDCT_US_2025_09_01:230253001 DOID:0060161 SBMA Spinobulbar Muscular Atrophy X-Linked Bulbo-Spinal Atrophy X-linked Spinal and Bulbar Muscular Atrophy spinal bulbar muscular atrophy X-linked recessive disease spinal muscular atrophy X-linked recessive inheritance ventral horn of spinal cord