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's subclass of is recorded as amyotrophic lateral sclerosis[4].
- FTDALS2's subclass of is recorded as frontotemporal dementia[5].
- FTDALS2's subclass of is recorded as FTDALS1[6].
- FTDALS2's subclass of is recorded as amyotrophic lateral sclerosis and frontotemporal dementia[7].
- FTDALS2's OMIM ID is recorded as 615911[8].
- FTDALS2's Disease Ontology ID is recorded as DOID:0060214[9].
- FTDALS2's genetic association is recorded as CHCHD10[10].
- FTDALS2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060214[11].
- FTDALS2's exact match is recorded as http://identifiers.org/doid/DOID:0060214[12].
- FTDALS2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_275872[13].
- FTDALS2's UMLS CUI is recorded as C4014648[14].
- FTDALS2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- FTDALS2's Mondo ID is recorded as MONDO_0014395[16].
- FTDALS2's UniProt disease ID is recorded as DI-04163[17].