Details of Disease | DrugMAP

General Information of Disease (ID: DISM2TT8)

Disease Name	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5
Synonyms	frontotemporal dementia and/or amyotrophic lateral sclerosis 5; FTDALS5
Disease Hierarchy	DISWZ9CJ: Familial amyotrophic lateral sclerosis DIS2B7L2: Frontotemporal dementia and/or amyotrophic lateral sclerosis DISM2TT8: Frontotemporal dementia and/or amyotrophic lateral sclerosis 5
Disease Identifiers	MONDO ID MONDO_0030875 UMLS CUI C5436884 OMIM ID 619141 MedGen ID 1756201

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CCNF	OTJFVU43	Strong	Autosomal dominant	[1]
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References

1	CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia. Nat Commun. 2016 Apr 15;7:11253. doi: 10.1038/ncomms11253.