FTDALS2
amyotrophic lateral sclerosis that has material basis in mutation in the CHCHD10 gene on chromosome 22. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis
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FTDALS2
Summary
FTDALS2 is a rare disease[1].
Key Facts
- FTDALS2's instance of is recorded as rare disease[2].
- FTDALS2's instance of is recorded as class of disease[3].
- FTDALS2 is a type of amyotrophic lateral sclerosis[4].
- FTDALS2 is a type of frontotemporal dementia[5].
- FTDALS2 is a type of FTDALS1[6].
- FTDALS2 is a type of amyotrophic lateral sclerosis and frontotemporal dementia[7].
- FTDALS2's genetic association is recorded as CHCHD10[8].
- FTDALS2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060214[9].
- FTDALS2's exact match is recorded as http://identifiers.org/doid/DOID:0060214[10].
- FTDALS2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_275872[11].
- FTDALS2's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].