symbol withdrawn MCKD1

Preferred Label : symbol withdrawn MCKD1;

Obsolete resource : true;

Approved symbol HGNC : MCKD1;

Alias symbols HGNC : ADMCKD1; MCKD; ADMCKD; MCD;

Chromosome HGNC : 1q21;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:6941;

Automatic exact mappings (from CISMeF team)
- Macular dystrophy, corneal [OMIM Phenotype]
- Tubulointerstitial kidney disease, autosomal dominant, 2 [OMIM Phenotype]
Replaced by
- mucin 1, cell surface associated [HGNC gene]

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