Preferred Name |
Muscular Atrophy, Spinal |
|
Synonyms |
Progressive Muscular Atrophies Adult Onset Spinal Muscular Atrophy |
|
Definitions |
A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089) |
|
ID |
http://purl.bioontology.org/ontology/MESH/D009134 |
|
altLabel |
Progressive Muscular Atrophies Motor Neuronopathy, Hereditary Neuronopathies, Hereditary Motor Spinal Amyotrophy Myelopathic Muscular Atrophy Spinal Muscular Atrophy, Distal Oculopharyngeal Spinal Muscular Atrophy Neuronopathy, Hereditary Motor Neuronopathies, Bulbospinal Atrophy, Progressive Muscular Adult Spinal Muscular Atrophy Amyotrophies, Spinal Muscular Atrophies, Progressive Spinal Muscular Atrophy, Oculopharyngeal Spinal Muscular Atrophy, Scapuloperoneal Form Myelopathic Muscular Atrophy, Progressive Amyotrophy, Spinal Scapuloperoneal Spinal Muscular Atrophy Bulbospinal Neuronopathy Adult-Onset Spinal Muscular Atrophy Neuronopathy, Bulbospinal Amyotrophy, Neurogenic Scapuloperoneal, New England Type Distal Spinal Muscular Atrophy Motor Neuronopathies, Hereditary Hereditary Motor Neuronopathies Bulbospinal Neuronopathies Atrophy, Spinal Muscular Progressive Myelopathic Muscular Atrophy Muscular Atrophy, Progressive Spinal Muscular Atrophy Hereditary Motor Neuronopathy Muscular Atrophy, Myelopathic Progressive Proximal Myelopathic Muscular Atrophy Progressive Muscular Atrophy Spinal Amyotrophies Proximal Myelopathic Muscular Atrophy, Progressive Atrophy, Myelopathic Muscular Muscular Atrophy, Adult Spinal Spinal Muscular Atrophy, Scapuloperoneal Scapuloperoneal Form of Spinal Muscular Atrophy Atrophies, Progressive Muscular Adult Onset Spinal Muscular Atrophy |
|
AN |
MUSCULAR ATROPHY, SPINAL, INFANTILE see SPINAL MUSCULAR ATROPHIES OF CHILDHOOD is also available |
|
AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
|
cui |
C0751335 C0751334 C0393547 C3661519 C0270765 C0393541 C0026847 C0393546 C0917981 |
|
DC |
1 |
|
definition |
A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089) |
|
DX |
19880101 |
|
HN |
1988 |
|
Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
Machine permutation |
1988 |
|
Mapped from |
http://purl.bioontology.org/ontology/MESH/C564506 http://purl.bioontology.org/ontology/MESH/C537968 http://purl.bioontology.org/ontology/MESH/C536881 http://purl.bioontology.org/ontology/MESH/C536880 http://purl.bioontology.org/ontology/MESH/C563948 http://purl.bioontology.org/ontology/MESH/C566673 http://purl.bioontology.org/ontology/MESH/C566670 http://purl.bioontology.org/ontology/MESH/C566674 http://purl.bioontology.org/ontology/MESH/C566675 http://purl.bioontology.org/ontology/MESH/C563443 http://purl.bioontology.org/ontology/MESH/C564807 http://purl.bioontology.org/ontology/MESH/C566695 http://purl.bioontology.org/ontology/MESH/C564626 http://purl.bioontology.org/ontology/MESH/C563981 http://purl.bioontology.org/ontology/MESH/C535715 http://purl.bioontology.org/ontology/MESH/C564362 http://purl.bioontology.org/ontology/MESH/C580044 http://purl.bioontology.org/ontology/MESH/C538417 http://purl.bioontology.org/ontology/MESH/C563561 |
|
MDA |
19870310 |
|
MMR |
20150623 |
|
MN |
C10.574.562.500 C10.228.854.468 C10.668.467.500 |
|
notation |
D009134 |
|
prefLabel |
Muscular Atrophy, Spinal |
|
TERMUI |
T812433 T027303 T369581 T369612 T369585 T369614 T369610 T027300 T369616 T812434 T842507 T842508 T812432 T752489 T752490 T369611 T369609 T369615 T369584 T369608 T369613 T027302 T027301 |
|
TH |
OMIM (2013) NLM (2000) UNK (19XX) NLM (2010) GHR (2014) NLM (1988) ORD (2010) |
|
tui |
T047 |
|
subClassOf |