Kennedy disease

Kennedy's disease, also known as bulbospinal muscular atrophy (BSMA), is a rare X-linked recessive motor neuron disease characterized by proximal and bulbar muscle wasting
rdfs:label
"Kennedy disease"@en
skos:altLabel
"Bulbospinal Muscular Atrophy, X-Linked"@en
"Bulbospinal Neuronopathy, X-Linked Recessive"@en
"Kennedy Disease"@en
"Kennedy Spinal and Bulbar Muscular Atrophy"@en
"Kennedy's disease"@en
"SBMA"@en
"SMAX1"@en
"SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1"@en
"SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1; SMAX1"@en
"Spinal and Bulbar Muscular Atrophy"@en
"Spinal and Bulbar Muscular Atrophy, X-Linked type 1"@en
"Spinal and bulbar muscular atrophy"@en
"Spinobulbar Muscular Atrophy"@en
"Spinobulbar muscular atrophy"@en
"X-Linked Bulbo-Spinal Atrophy"@en
"X-linked BSMA"@en
"X-linked Spinal and Bulbar Muscular Atrophy"@en
"X-linked bulbospinal amyotrophy"@en
"X-linked bulbospinal muscular atrophy"@en
"spinal bulbar muscular atrophy"@en
schema:description
"Kennedy's disease, also known as bulbospinal muscular atrophy (BSMA), is a rare X-linked recessive motor neuron disease characterized by proximal and bulbar muscle wasting"@en
schema:dateModified "2026-10-24T00:23:12+00:00"^^xsd:dateTime
schema:version 2560165325
wikibase:identifiers 32
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p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060161>
wdt:P10283 "C2780434838"
wdt:P11143 "Spinal and bulbar muscular atrophy"
wdt:P11430 "DI-01053"
wdt:P1193 0.00005^^xsd:decimal
wdt:P1325 <http://www.nanbyou.or.jp/entry/73>
wdt:P138 William Kennedy
wdt:P14914 "D00481"
wdt:P1550 "481"
wdt:P1748 "C85233"
wdt:P1995 neurology
wdt:P2293 AR
wdt:P279 nervous system heredodegenerative disease
X-linked recessive disease
bulbospinal muscular atrophy of adult
rare male infertility due to testicular endocrine disorder
wdt:P2841 adult onset
wdt:P2888 <http://identifiers.org/doid/DOID:0060161>
<http://purl.obolibrary.org/obo/DOID_0060161>
<http://www.orpha.net/ORDO/Orphanet_481>
wdt:P2892 "C0393547"
"C0752353"
"C1839259"
"C2931395"
wdt:P31 type of disease
designated intractable/rare disease
rare disease
wdt:P3417 "Kennedys-Disease"
wdt:P373 "Spinal and bulbar muscular atrophy"
wdt:P4229 "G12.2"
wdt:P4233 "kennedy-s-disease"
wdt:P4317 "6818"
wdt:P486 "D055534"
wdt:P492 "313200"
wdt:P493 "335.1"
wdt:P494 "G12.1"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0010735"
wdt:P557 "7144"
wdt:P6366 "2780434838"
wdt:P646 "/m/073pw6"
wdt:P6532 hyporeflexia
lipid metabolism disorder
skeletal muscle atrophy
hypotonia
dysarthria
movement disorders
type 2 diabetes
gynecomastia
microorchidism
gait abnormality
dysphonia
wdt:P665 "H00062"
wdt:P668 "NBK1333"
wdt:P672 "C10.228.854.468.399"
"C10.574.500.175"
"C10.574.562.500.374"
"C10.668.467.500.186"
"C16.320.322.076"
"C16.320.400.100"
wdt:P673 "1172604"
wdt:P691 "ph902286"
wdt:P699 "DOID:0060161"
wdt:P7464 "spinal-and-bulbar-muscular-atrophy"
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