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
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 - -
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