loading...| Preferred Name |
Muscular Atrophy, Spinal |
| Synonyms |
Neuronopathies, Hereditary Motor |
| 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 |
Neuronopathies, Hereditary Motor Progressive Muscular Atrophies Adult Spinal Muscular Atrophy Neuronopathy, Bulbospinal Muscular Atrophy, Myelopathic Bulbospinal Neuronopathy Atrophy, Spinal Muscular Spinal Muscular Atrophy Atrophy, Progressive Muscular Amyotrophy, Spinal Bulbospinal Neuronopathies Motor Neuronopathies, Hereditary Myelopathic Muscular Atrophy, Progressive Neuronopathies, Bulbospinal Progressive Muscular Atrophy Scapuloperoneal Form of Spinal Muscular Atrophy Myelopathic Muscular Atrophy Proximal Myelopathic Muscular Atrophy, Progressive Adult Onset Spinal Muscular Atrophy Amyotrophy, Neurogenic Scapuloperoneal, New England Type Spinal Muscular Atrophy, Oculopharyngeal Spinal Muscular Atrophy, Scapuloperoneal Form Adult-Onset Spinal Muscular Atrophy Oculopharyngeal Spinal Muscular Atrophy Neuronopathy, Hereditary Motor Spinal Amyotrophy Muscular Atrophy, Adult Spinal Progressive Myelopathic Muscular Atrophy Atrophy, Myelopathic Muscular Spinal Muscular Atrophy, Distal Progressive Proximal Myelopathic Muscular Atrophy Spinal Muscular Atrophy, Scapuloperoneal Atrophies, Progressive Muscular Distal Spinal Muscular Atrophy Hereditary Motor Neuronopathies Muscular Atrophies, Progressive Hereditary Motor Neuronopathy Amyotrophies, Spinal Muscular Atrophy, Progressive Spinal Amyotrophies Scapuloperoneal Spinal Muscular Atrophy Motor Neuronopathy, Hereditary |
| 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 |
C0393541 C0917981 C0393546 C0751335 C3661519 C0751334 C0393547 C0270765 C0026847 |
| 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/Q000401 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000523 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000652 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000209 |
| Machine permutation |
1988 |
| Mapped from |
http://purl.bioontology.org/ontology/MESH/C536880 http://purl.bioontology.org/ontology/MESH/C566673 http://purl.bioontology.org/ontology/MESH/C566670 http://purl.bioontology.org/ontology/MESH/C563443 http://purl.bioontology.org/ontology/MESH/C567084 http://purl.bioontology.org/ontology/MESH/C563562 http://purl.bioontology.org/ontology/MESH/C535715 http://purl.bioontology.org/ontology/MESH/C563948 http://purl.bioontology.org/ontology/MESH/C564362 http://purl.bioontology.org/ontology/MESH/C563561 http://purl.bioontology.org/ontology/MESH/C580044 http://purl.bioontology.org/ontology/MESH/C566674 http://purl.bioontology.org/ontology/MESH/C564506 http://purl.bioontology.org/ontology/MESH/C536881 http://purl.bioontology.org/ontology/MESH/C563981 http://purl.bioontology.org/ontology/MESH/C537968 http://purl.bioontology.org/ontology/MESH/C564807 http://purl.bioontology.org/ontology/MESH/C564626 http://purl.bioontology.org/ontology/MESH/C566695 |
| MDA |
19870310 |
| MMR |
20150623 |
| MN |
C10.668.467.500 C10.574.562.500 C10.228.854.468 |
| notation |
D009134 |
| prefLabel |
Muscular Atrophy, Spinal |
| TERMUI |
T369609 T369581 T812434 T027301 T369611 T752490 T369610 T369616 T369612 T369614 T369608 T027303 T812433 T369615 T812432 T369585 T369613 T842507 T027302 T842508 T752489 T369584 T027300 |
| TH |
UNK (19XX) NLM (2000) NLM (2010) ORD (2010) NLM (1988) OMIM (2013) GHR (2014) |
| tui |
T047 |
| subClassOf |