Human genes for Kennedy's disease
Kennedy's disease [DOID:0060161]
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.
Synonyms: Kennedy's disease, DOID:0060161, Kennedys disease, Kennedy's disorder, Kennedy's syndrome ...
Linkouts: OMIM