amyotrophic lateral sclerosis 7

Preferred Label : amyotrophic lateral sclerosis 7;

Obsolete resource : true;

Approved symbol HGNC : ALS7;

Chromosome HGNC : 20p13;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:34539;

UMLS CUI

C2681918;

Automatic exact mappings (from CISMeF team)
- Amyotrophic lateral sclerosis 7 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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