Amyotrophic Lateral Sclerosis 21 (ALS21)

Amyotrophic Lateral Sclerosis 21(来自ICD-11)

别称:

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

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

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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