spastic paraplegia 29 (autosomal dominant)

Preferred Label : spastic paraplegia 29 (autosomal dominant);

Obsolete resource : true;

Approved symbol HGNC : SPG29;

Chromosome HGNC : 1p31.1-p21.1;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:30161;

UMLS CUI

C1823101;

Automatic exact mappings (from CISMeF team)
- Spastic paraplegia 29, autosomal dominant [OMIM Phenotype]
Orphanet gene
- spastic paraplegia 29 (autosomal dominant) [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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