All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04552 - hydroxykynureninuria? 236800 AR 1 1 KYNU - -
05031 CATMANS Catel-Manzke syndrome (CATMANS) 616145 AR 4 4 KYNU, TGDS - -
05299 MFM myopathy, myofibrillar (MFM) - - 96 95 KY - -
05787 MFM7 myopathy, myofibrillar, type 7 (MFM7) 617114 AR - - KY - -
05680 VCRL vertebral, cardiac, renal, and limb defects syndrome (VCRL) - XLR - - HAAO, KYNU, NADSYN1 - -
05682 VCRL2 vertebral, cardiac, renal, and limb defects syndrome, type 2 (VCRL2) 617661 AR - - KYNU - -
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