symbol withdrawn SPG23

Preferred Label : symbol withdrawn SPG23;

Obsolete resource : true;

Approved symbol HGNC : SPG23;

Chromosome HGNC : 1q24-q32;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:21340;

UMLS CUI

C1427494;

Automatic exact mappings (from CISMeF team)
- Spastic paraplegia 23, autosomal recessive [OMIM Phenotype]
Orphanet gene
- spastic paraplegia 23 (autosomal recessive) [ORDO Gene]
Replaced by
- dual serine/threonine and tyrosine protein kinase [HGNC gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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