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Tremor, hereditary essential, 4
Any essential tremor in which the cause of the disease is a mutation in the FUS gene. [from MONDO]
Amyotrophic lateral sclerosis type 6
A neurodegenerative disease with characteristics of progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. Caused by heterozygous mutation in the FUS gene on chromosome 16p11. [from SNOMEDCT_US]
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