amyotrophic lateral sclerosis type 16
amyotrophic lateral sclerosis that has material basis in mutation in the SIGMAR1 gene (SETX) on chromosome 9
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amyotrophic lateral sclerosis type 16
Summary
amyotrophic lateral sclerosis type 16 is a rare disease[1].
Key Facts
- amyotrophic lateral sclerosis type 16's instance of is recorded as rare disease[2].
- amyotrophic lateral sclerosis type 16's instance of is recorded as class of disease[3].
- amyotrophic lateral sclerosis type 16's subclass of is recorded as amyotrophic lateral sclerosis[4].
- amyotrophic lateral sclerosis type 16's subclass of is recorded as familial amyotrophic lateral sclerosis[5].
- amyotrophic lateral sclerosis type 16's OMIM ID is recorded as 614373[6].
- amyotrophic lateral sclerosis type 16's Disease Ontology ID is recorded as DOID:0060207[7].
- amyotrophic lateral sclerosis type 16's genetic association is recorded as SIGMAR1[8].
- amyotrophic lateral sclerosis type 16's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060207[9].
- amyotrophic lateral sclerosis type 16's exact match is recorded as http://identifiers.org/doid/DOID:0060207[10].
- amyotrophic lateral sclerosis type 16's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_300605[11].
- amyotrophic lateral sclerosis type 16's UMLS CUI is recorded as C3280587[12].
- amyotrophic lateral sclerosis type 16's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- amyotrophic lateral sclerosis type 16's Mondo ID is recorded as MONDO_0013715[14].
- amyotrophic lateral sclerosis type 16's UniProt disease ID is recorded as DI-03324[15].