FTDALS3
amyotrophic lateral sclerosis that has material basis in mutation in the SQSTM1 gene on chromosome 5q35
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FTDALS3
Summary
FTDALS3 is a class of disease[1].
Key Facts
- FTDALS3's instance of is recorded as class of disease[2].
- FTDALS3's subclass of is recorded as amyotrophic lateral sclerosis[3].
- FTDALS3's subclass of is recorded as frontotemporal dementia[4].
- FTDALS3's subclass of is recorded as behavioral variant of frontotemporal dementia[5].
- FTDALS3's subclass of is recorded as FTDALS1[6].
- FTDALS3's subclass of is recorded as amyotrophic lateral sclerosis and frontotemporal dementia[7].
- FTDALS3's OMIM ID is recorded as 616437[8].
- FTDALS3's Disease Ontology ID is recorded as DOID:0110068[9].
- FTDALS3's genetic association is recorded as SQSTM1[10].
- FTDALS3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110068[11].
- FTDALS3's exact match is recorded as http://identifiers.org/doid/DOID:0110068[12].
- FTDALS3's UMLS CUI is recorded as C4225326[13].
- FTDALS3's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- FTDALS3's Mondo ID is recorded as MONDO_0014640[15].
- FTDALS3's UniProt disease ID is recorded as DI-04471[16].