amyotrophic lateral sclerosis type 19
amyotrophic lateral sclerosis that has material basis in mutation in the ERBB4 gene on chromosome 2
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amyotrophic lateral sclerosis type 19
Summary
amyotrophic lateral sclerosis type 19 is a class of disease[1].
Key Facts
- amyotrophic lateral sclerosis type 19's instance of is recorded as class of disease[2].
- amyotrophic lateral sclerosis type 19's subclass of is recorded as amyotrophic lateral sclerosis[3].
- amyotrophic lateral sclerosis type 19's subclass of is recorded as familial amyotrophic lateral sclerosis[4].
- amyotrophic lateral sclerosis type 19's OMIM ID is recorded as 615515[5].
- amyotrophic lateral sclerosis type 19's Disease Ontology ID is recorded as DOID:0060210[6].
- amyotrophic lateral sclerosis type 19's genetic association is recorded as ERBB4[7].
- amyotrophic lateral sclerosis type 19's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060210[8].
- amyotrophic lateral sclerosis type 19's exact match is recorded as http://identifiers.org/doid/DOID:0060210[9].
- amyotrophic lateral sclerosis type 19's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_803[10].
- amyotrophic lateral sclerosis type 19's UMLS CUI is recorded as C3715155[11].
- amyotrophic lateral sclerosis type 19's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- amyotrophic lateral sclerosis type 19's Mondo ID is recorded as MONDO_0014223[13].
- amyotrophic lateral sclerosis type 19's UniProt disease ID is recorded as DI-03940[14].