symbol withdrawn NBIA1

Preferred Label : symbol withdrawn NBIA1;

Obsolete resource : true;

Approved symbol HGNC : NBIA1;

Alias symbols HGNC : FLJ11729; HSS; PKAN;

Chromosome HGNC : 20p13-p12.3;

Locus type HGNC : other;

Details

Origin ID

HGNC:7649;

Automatic exact mappings (from CISMeF team)
- Hallermann-streiff syndrome [OMIM Phenotype]
- Neurodegeneration with brain iron accumulation 1 [OMIM Phenotype]
Replaced by
- pantothenate kinase 2 [HGNC gene]

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