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GTR Home > Conditions/Phenotypes > Amyotrophic lateral sclerosis type 9

Summary

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 angiogenin gene (ANG) on chromosome 14q11. [from SNOMEDCT_US]

Genes See tests for all associated and related genes

  • Also known as: ALS9, HEL168, RAA1, RNASE4, RNASE5, ANG
    Summary: angiogenin

Clinical features

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