All diseases

10 entries on 1 page. Showing entries 1 - 10.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02656 ARVD8 dysplasia, ventricular, right, arrhythmogenic, type 8 (ARVD-8) 607450 AD - - DSP - -
02560 DCWHK cardiomyopathy, dilated with woolly hair and keratoderma (DCWHK, Carvajal syndrome) 605676 AR - - DSP - autosomal recessive
04453 DCWHKTA cardiomyopathy, dilated with woolly hair, keratoderma, and tooth agenesis (DCWHKTA) 615821 AD - - DSP - -
00445 DFNA39 deafness, autosomal dominant, type 39, with dentinogenesis (DFNA-39) 605594 AD 1 1 DSPP - -
00443 DGI1 dentinogenesis imperfecta, Shields type I (DGI-1) 125490 AD 30 22 DSPP - -
00442 DGI3 dentinogenesis imperfecta, Shields type III (DGI-3) 125500 AD 1 1 DSPP - -
00444 DTDP2 dysplasia, dentin, type 2 (DTDP-2) 125420 AD 8 8 DSPP - -
02868 EBLA epidermolysis bullosa, lethal acantholytic (EBLA) 609638 AR - - DSP - autosomal recessive
03202 PPKS2 keratosis palmoplantaris striata, type 2 (PPKS-2) 612908 AD - - DSP - -
02687 SFWHS skin fragility, woolly hair syndrome (SFWHS) 607655 AR - - DSP - autosomal recessive
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