Kennedy disease
Also known as Kennedy's disease, SBMA, SMAX1, X-linked BSMA+13 more
Kennedy's disease, SBMA, SMAX1, X-linked BSMA, X-linked bulbo-spinal atrophy, X-linked bulbospinal amyotrophy, X-linked bulbospinal muscular atrophy, X-linked spinal and bulbar muscular atrophy, spinal and bulbar muscular atrophy of Kennedy, X-linked recessive, spinal and bulbar muscular atrophy, X-linked type 1, spinal bulbar muscular atrophy, spinobulbar muscular atrophy, Kennedy spinal and bulbar muscular atrophy, bulbospinal muscular atrophy, X-linked, bulbospinal neuronopathy, X-linked recessive, spinal and bulbar muscular atrophy, spinal and bulbar muscular atrophy, X-linked 1.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
Kennedy's disease, SBMA, SMAX1, X-linked BSMA, X-linked bulbo-spinal atrophy, X-linked bulbospinal amyotrophy, X-linked bulbospinal muscular atrophy, X-linked spinal and bulbar muscular atrophy, spinal and bulbar muscular atrophy of Kennedy, X-linked recessive, spinal and bulbar muscular atrophy, X-linked type 1, spinal bulbar muscular atrophy, spinobulbar muscular atrophy, Kennedy spinal and bulbar muscular atrophy, bulbospinal muscular atrophy, X-linked, bulbospinal neuronopathy, X-linked recessive, spinal and bulbar muscular atrophy, spinal and bulbar muscular atrophy, X-linked 1
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.