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Amyotrophic lateral sclerosis

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Description

A neurodegenerative disease characterized by progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord.

ORDO

  • Mode of Inheritance

    VARIANTS

    86

    SEE THE VARIANTS →

    Genes

    External Links

    • OMIM
    • Orphanet

      803

    • HPO

      4723

    • Medgen

      C0002736

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