All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05342 CAKUT kidney and urinary tract, anomalies, congenital (CAKUT) - - 212 212 CHRNA3, DSTYK, FOXD2, SLIT3, TBX18 - -
02984 CAKUT1;RHDNS1 kidney and urinary tract, anomalies, congenital, susceptibility to, type 1 (CAKUT-1, renal hypodysplasia, nonsyndromic, type 1 (RHDNS-1)) 610805 AD - - DSTYK - -
03941 EBSB2 epidermolysis bullosa simplex, autosomal recessive, type 2 (EBSB-2) 615425 AR - - DST - -
03695 HSAN6 neuropathy, sensory and autonomic, hereditary, type VI (HSAN-6) 614653 AR - - DST - -
04591 MRT46 mental retardation, autosomal recessive, type 46 (MRT-45) 616116 AR 1 1 NDST1 - -
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