symbol withdrawn RSMD1

Preferred Label : symbol withdrawn RSMD1;

Obsolete resource : true;

Approved symbol HGNC : RSMD1;

Alias symbols HGNC : RSS;

Chromosome HGNC : 1p36-p35;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:10460;

Automatic exact mappings (from CISMeF team)
- Congenital myopathy 3 with rigid spine [OMIM Phenotype]
Replaced by
- selenoprotein N [HGNC gene]

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