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
01321 - erythromelalgia, primary 133020 AD 31 31 SCN9A - -
01872 CIP;HSAN2D pain, indifference, congenital, autosomal recessive (CIP) 243000 AR 17 15 SCN9A - autosomal recessive
03473 GEFSP7 epilepsy, generalized, with febrile seizures plus, type 7 (GEFSP-7) 613863 AD 1 - SCN9A - autosomal dominant
01487 PEXPD pain disorder, paroxysmal, extreme (PEXPD) 167400 AD 2 2 SCN9A - autosomal dominant
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