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
06539 ECTD13 Ectodermal dysplasia 13, hair/tooth type 617392 AR 2 2 KREMEN1 - -
05108 ECTDO dysplasia, ectodermal, with oligodontia (ECTDO) - - 4 4 KREMEN1 - -
00426 MEN1 neoplasia, endocrine, multiple, type 1 (MEN-1, Wermer syndrome) 131100 AD 542 549 MEN1 - autosomal dominant
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