OBO ID: DOID:0060161 |
Term Name: | Kennedy's disease | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0060161 ) |
OTHER Kennedy's disease PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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