symbol withdrawn MCDR2

Preferred Label : symbol withdrawn MCDR2;

Obsolete resource : true;

Approved symbol HGNC : MCDR2;

Chromosome HGNC : 4p16.3-p15.2;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:18438;

Automatic exact mappings (from CISMeF team)
- Macular dystrophy, retinal, 2 [OMIM Phenotype]
Replaced by
- prominin 1 [HGNC gene]

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