Amyotrophic Lateral Sclerosis 21 (ALS21)
Alias:
Amyotrophic Lateral Sclerosis Type 21
Als21
Multisystem Proteinopathy 5
Msp5
Vocal Cord and Pharyngeal Dysfunction with Distal Myopathy, Formerly
Vocal Cord and Pharyngeal Dysfunction with Distal Myopathy
Distal Myopathy with Vocal Cord Weakness
Sclerosis, Lateral, Amyotrophic, Type 21
Myopathy, Distal, 2, Formerly
Myopathy, Distal 2
Distal Myopathy 2
Vcpdm, Formerly
Mpd2, Formerly
Vcpdm
Mpd2
Amyotrophic Lateral Sclerosis 21, also known as amyotrophic lateral sclerosis type 21, is related to distal myopathy 2 and distal hereditary motor neuronopathy type 7, and has symptoms including upper motor neuron signs An important gene associated with Amyotrophic Lateral Sclerosis 21 is MATR3 (Matrin 3), and among its related pathways/superpathways is Amyotrophic lateral sclerosis (ALS). Affiliated tissues include spinal cord and skeletal muscle, and related phenotypes are dementia and distal sensory impairment
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