symbol withdrawn KFSD

Preferred Label : symbol withdrawn KFSD;

Obsolete resource : true;

Approved symbol HGNC : KFSD;

Chromosome HGNC : Xp22.2-p21.2;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:6313;

Automatic exact mappings (from CISMeF team)
- Keratosis follicularis spinulosa decalvans, autosomal dominant [OMIM Phenotype]
Replaced by
- membrane bound transcription factor peptidase, site 2 [HGNC gene]

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