All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04551 - cirrhosis, cryptogenic, susceptibility to 215600 AR - - KRT18, KRT8 - -
05728 ECTD dysplasia, ectodermal (ECTD) - - 60 59 CST6, KRT85 - -
02408 ECTD4 dysplasia, ectodermal, type 4, hair/nail (ECTD-4) 602032 AR - - KRT85 - -
07050 EKVP erythrokeratodermia variabilis et progressiva - - - - KRT83 - -
06180 EKVP5 erythrokeratodermia variabilis et progressiva, type 5 617756 AR - - KRT83 - -
01443 MNLIX Monilethrix 158000 AD 48 47 KRT81, KRT83, KRT86 - -
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