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Summary Literature (0)
MIM:614696 - MOVED TO 600795

Xenbase Genes: chmp2b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0005144 - familial amyotrophic lateral sclerosis
MONDO:0010936 - frontotemporal dementia and/or amyotrophic lateral sclerosis 7
MONDO:0013861 - obsolete amyotrophic lateral sclerosis type 17