amyotrophic lateral sclerosis type 20
amyotrophic lateral sclerosis with juvenile onset that has material basis in mutation in the HNRNPA1 gene on chromosome 12
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amyotrophic lateral sclerosis type 20
Summary
amyotrophic lateral sclerosis type 20 is a class of disease[1].
Key Facts
- amyotrophic lateral sclerosis type 20's instance of is recorded as class of disease[2].
- amyotrophic lateral sclerosis type 20's subclass of is recorded as amyotrophic lateral sclerosis[3].
- amyotrophic lateral sclerosis type 20's subclass of is recorded as familial amyotrophic lateral sclerosis[4].
- amyotrophic lateral sclerosis type 20's OMIM ID is recorded as 615426[5].
- amyotrophic lateral sclerosis type 20's Disease Ontology ID is recorded as DOID:0060211[6].
- amyotrophic lateral sclerosis type 20's genetic association is recorded as HNRNPA1[7].
- amyotrophic lateral sclerosis type 20's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060211[8].
- amyotrophic lateral sclerosis type 20's exact match is recorded as http://identifiers.org/doid/DOID:0060211[9].
- amyotrophic lateral sclerosis type 20's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_803[10].
- amyotrophic lateral sclerosis type 20's UMLS CUI is recorded as C3715156[11].
- amyotrophic lateral sclerosis type 20's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- amyotrophic lateral sclerosis type 20's Mondo ID is recorded as MONDO_0014181[13].
- amyotrophic lateral sclerosis type 20's UniProt disease ID is recorded as DI-03881[14].