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
02783 APLD lipodystrophy, partial, acquired, susceptibility to 608709 AD - - LMNB2 - -
06406 EPM9 epilepsy, progressive myoclonic, type 9 616540 AR - - LMNB2 - -
07163 MCPH27 microcephaly, type 27, primary, autosomal dominant 619180 AD - - LMNB2 - -
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