All diseases

3 entries on 1 page. Showing entries 1 - 3.
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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 - -
02572 CDG2B glycosylation, congenital disorder of, type IIb (CDG-2B) 606056 AR - - MOGS - -
03587 NRCLP7 narcolepsy, type 7 (NRCLP-7) 614250 AD - - MOG - -
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