All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01321 - erythromelalgia, primary 133020 - 31 31 SCN9A - -
01872 CIP pain, indifference, congenital, autosomal recessive (CIP) 243000 - 16 15 SCN9A - autosomal recessive
00353 EIEE-6 encephalopathy, epileptic, early infantile, type 6 (EIEE-6, Dravet syndrome) 607208 - 26 26 SCN1A, SCN9A - -
03473 GEFSP-7 epilepsy, generalized, with febrile seizures plus, type 7 (GEFSP-7) 613863 - 1 0 SCN9A - autosomal dominant
01487 PEPD pain disorder, paroxysmal, extreme (PEPD) 167400 - 2 2 SCN9A - autosomal dominant
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