amyotrophic lateral sclerosis 3 (autosomal dominant)

Preferred Label : amyotrophic lateral sclerosis 3 (autosomal dominant);

Obsolete resource : true;

Approved symbol HGNC : ALS3;

Chromosome HGNC : 18q21;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:444;

UMLS CUI

C1412368;

Automatic exact mappings (from CISMeF team)
- Amyotrophic lateral sclerosis 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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