View diseases

15 entries on 1 page. Showing entries 1 - 15.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes
00009 ALMS Alstrom Disease - 0 0 -
00006 CD Chondrodysplasia - 0 0 -
00011 EPS Epilepsy - 0 0 -
00014 GrowthRet Growth Retardation - 0 0 -
00015 HerCan Hereditary Cancer - 0 0 -
00003 HI Hearing Impairment - 0 0 -
00004 IEM Inherited Metabolic Disorder - 0 0 -
00005 MD Motor Disorder - 0 0 -
00001 MR Mental Retardation - 0 0 -
00007 MusD Muscular Dystrophy - 0 0 -
00013 NeurDis Neurologic Disorder - 0 0 -
00012 RenDis Renal Disorder - 0 0 -
00008 SKN Skin Disorder - 0 0 -
00010 SKT Skeletal Disorder - 0 0 -
00002 VI Vision Impairment - 0 0 -