Spinal Muscular Atrophy (SMA)
Alias:
Sma - [spinal Muscular Atrophy]
Hereditary Motor Neuronopathy
Progressive Muscular Atrophy
Spinal Muscle Degeneration
Atrophy, Muscular, Spinal
Muscular Atrophy Spinal
Spinal Muscle Wasting
Spinal Amyotrophies
Sma-Associated Sma
Spinal Amyotrophy
Proximal Sma
5q Sma
Sma
Basic Information
Medical Symptom
Gene & Mutation
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References
Spinal Muscular Atrophy, also known as sma - [spinal muscular atrophy], is related to spinal muscular atrophy, x-linked 2 and spinal muscular atrophy, type i, and has symptoms including back pain, headache and pain. An important gene associated with Spinal Muscular Atrophy is SMN1 (Survival Of Motor Neuron 1, Telomeric), and among its related pathways/superpathways is SARS-CoV-2 modulates host translation machinery. The drugs Acetaminophen and Risdiplam have been mentioned in the context of this disorder. Affiliated tissues include spinal cord and skeletal muscle, and related phenotypes are nervous system and normal
Related ID:
MESH:D009134
ICD11:71074342
Basic Information
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MALACARDS
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Unknown
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6
49
100
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Comparison
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