MeSH Browser

MeSH Heading: Bulbo-Spinal Atrophy, X-Linked
Tree Number(s): 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
Unique ID: D055534
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D055534
Scope Note: An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
Entry Term(s): Atrophy, Muscular, Spinobulbar; Bulbospinal Muscular Atrophy, X-linked; Kennedy Disease; Kennedy Spinal and Bulbar Muscular Atrophy; Kennedy Syndrome; Kennedy's Disease; Muscular Atrophy, Spinobulbar; Spinal And Bulbar Muscular Atrophy, X-Linked 1; Spinal and Bulbar Muscular Atrophy; Spinobulbar Muscular Atrophy; X-Linked Bulbo-Spinal Atrophy; X-Linked Spinal and Bulbar Muscular Atrophy; X-linked Bulbospinal Muscular Atrophy
Public MeSH Note: 2009; see MUSCULAR ATROPHY, SPINAL 2000-2008
History Note: 2009(2000); use MUSCULAR ATROPHY, SPINAL 2000-2008
Date Established: 2009/01/01
Date of Entry: 2008/07/08
Revision Date: 2018/06/29

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Bulbo-Spinal Atrophy, X-Linked MeSH Descriptor Data 2025