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
02159 - epilepsy, X-linked, with variable learning disabilities and behavior disorders 300491 XLD;XLR 1 1 SYN1 - -
05680 VCRL vertebral, cardiac, renal, and limb defects syndrome (VCRL) - XLR - - HAAO, KYNU, NADSYN1 - -
05882 VCRL3 vertebral, cardiac, renal, and limb defects syndrome, type 3 (VCRL3) 618845 AR - - NADSYN1 - -
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