|OBO ID: DOID:0060161|
|Term Name:||Kennedy's disease||Search Ontology:|
|Definition:||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. http://en.wikipedia.org/wiki/Kennedy_disease|
|Ontology:||Human Disease (DOID:0060161)|
OTHER Kennedy's disease PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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