All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05461 CDG glycosylation, congenital disorder of (CDG) - - 86 82 CAMLG, DHRSX, EDEM3, MAN2C1, MOGS, NUS1, SLC39A8, STT3A, STT3B, UGGT1 - -
05354 glutathioninuria glutathioninuria (gamma-glutamyltranspeptidase deficiency) 231950 AR 1 1 GGT1 - autosomal recessive
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