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
02677 CIEHK ichthyosis, cyclic, with epidermolytic hyperkeratosis 607602 AD 51 51 KRT1, KRT10 - -
02829 CRIE;IWC erythroderma, ichthyosiform, congenital reticular (CRIE, ichthyosis with confetti (IWC)) 609165 AD - - KRT10 - -
01216 EHK;BIE epidermolytic hyperkeratosis (EHK, bullous ichthyosiform erythroderma (BIE)) 113800 AD;AR - - KRT1, KRT10 - -
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