amyotrophic lateral sclerosis type 21
amyotrophic lateral sclerosis that has material basis in mutation in the MATR3 gene on chromosome 5
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amyotrophic lateral sclerosis type 21
Summary
amyotrophic lateral sclerosis type 21 is a class of disease[1].
Key Facts
- amyotrophic lateral sclerosis type 21's instance of is recorded as class of disease[2].
- amyotrophic lateral sclerosis type 21's subclass of is recorded as amyotrophic lateral sclerosis[3].
- amyotrophic lateral sclerosis type 21's subclass of is recorded as nervous system heredodegenerative disease[4].
- amyotrophic lateral sclerosis type 21's OMIM ID is recorded as 606070[5].
- amyotrophic lateral sclerosis type 21's Disease Ontology ID is recorded as DOID:0060212[6].
- amyotrophic lateral sclerosis type 21's NCI Thesaurus ID is recorded as C168755[7].
- amyotrophic lateral sclerosis type 21's genetic association is recorded as MATR3[8].
- amyotrophic lateral sclerosis type 21's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060212[9].
- amyotrophic lateral sclerosis type 21's exact match is recorded as http://identifiers.org/doid/DOID:0060212[10].
- amyotrophic lateral sclerosis type 21's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_600[11].
- amyotrophic lateral sclerosis type 21's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_803[12].
- amyotrophic lateral sclerosis type 21's UMLS CUI is recorded as C1853723[13].
- amyotrophic lateral sclerosis type 21's UMLS CUI is recorded as C3807521[14].
- amyotrophic lateral sclerosis type 21's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- amyotrophic lateral sclerosis type 21's Mondo ID is recorded as MONDO_0011632[16].
- amyotrophic lateral sclerosis type 21's UniProt disease ID is recorded as DI-02625[17].