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
07109 CMYO18 myopathy, congenital, type 18, due to dihydropyridine receptor defect 620246 AD;AR - - CACNA1S - -
01500 HOKPP paralysis, hypokalemic, periodic (HOKPP) - - 13 14 CACNA1S, SCN4A - -
05437 HOKPP1 paralysis, hypokalemic, periodic, type 1 170400 AD 1 1 CACNA1S - autosomal dominant
05449 MHS hyperthermia, malignant, susceptibility (MHS) - - 463 464 CACNA1S, RYR1 - -
02401 MHS5 hyperthermia, malignant, susceptibility, type 5 (MHS-5) 601887 AD 2 2 CACNA1S - autosomal dominant
01585 TTPP1 Thyrotoxic periodic paralysis 188580 AD - - CACNA1S - -
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