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
04437 DFNB66 deafness?, autosomal recessive, type 66 (DFNB-66) 610212 AR 0 0 DCDC2 - -
04438 NPHP19 nephronophthisis, type 19 (NPHP-19) 616217 AR 0 0 DCDC2 - -
06700 NSC Sclerosing cholangitis, neonatal 617394 AR 0 0 DCDC2 - -
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