All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06255 BAIPRCK Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT 191800 AR - - CHRNA3 - -
05342 CAKUT kidney and urinary tract, anomalies, congenital (CAKUT) - - 212 212 CHRNA3, DSTYK, FOXD2, SLIT3, TBX18 - -
05259 SQTL smoking, quantitative trait locus (SQTL) - - 2 2 CHRNA3 - -
03083 SQTL3 smoking, quantitative trait locus 3 (SQTL-3) 612052 - - - CHRNA3, CHRNA5 - -
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