amyotrophic lateral sclerosis type 18
amyotrophic lateral sclerosis that has material basis in mutation in the PFN1 gene on chromosome 17
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amyotrophic lateral sclerosis type 18
Summary
amyotrophic lateral sclerosis type 18 is a class of disease[1].
Key Facts
- amyotrophic lateral sclerosis type 18's instance of is recorded as class of disease[2].
- amyotrophic lateral sclerosis type 18's subclass of is recorded as amyotrophic lateral sclerosis[3].
- amyotrophic lateral sclerosis type 18's subclass of is recorded as familial amyotrophic lateral sclerosis[4].
- amyotrophic lateral sclerosis type 18's OMIM ID is recorded as 614808[5].
- amyotrophic lateral sclerosis type 18's Disease Ontology ID is recorded as DOID:0060209[6].
- amyotrophic lateral sclerosis type 18's genetic association is recorded as PFN1[7].
- amyotrophic lateral sclerosis type 18's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060209[8].
- amyotrophic lateral sclerosis type 18's exact match is recorded as http://identifiers.org/doid/DOID:0060209[9].
- amyotrophic lateral sclerosis type 18's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_803[10].
- amyotrophic lateral sclerosis type 18's UMLS CUI is recorded as C3553719[11].
- amyotrophic lateral sclerosis type 18's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- amyotrophic lateral sclerosis type 18's Mondo ID is recorded as MONDO_0013891[13].
- amyotrophic lateral sclerosis type 18's UniProt disease ID is recorded as DI-03520[14].