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
02572 CDG-2B glycosylation, congenital disorder of, type IIb (CDG-2B) 606056 - - - MOGS - -
03587 NRCLP-7 narcolepsy, type 7 (NRCLP-7) 614250 - - - MOG - -
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