All diseases

8 entries on 1 page. Showing entries 1 - 8.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03516 ATFB10 fibrillation, atrial, familial, type 10 614022 - 2 2 SCN5A - -
00118 BRGDA1 Brugada syndrome, type 1 (BRGDA-1) 601144 AD 366 365 SCN5A - -
02343 CMD1E cardiomyopathy, dilated, type 1E (CMD-1E) 601154 AD - - SCN5A - -
00407 LQT3 QT syndrome, long, type 3 (LQT-3) 603830 AD 74 72 SCN5A - -
01217 PFHB1A heart block, progressive, familial, type 1A (PFHB1A, heart block, nonprogressive) 113900 AD 4 4 SCN5A - -
02087 SIDS death, sudden, syndrome, infant (SIDS) 272120 AR 126 126 SCN5A - -
02765 SSS1 sinus, sick, syndrome, type 1, autosomal recessive (SSS-1) 608567 AR - - SCN5A - -
02468 VF1 fibrillation, ventricular, paroxysmal, familial, type 1 (VF-1) 603829 - 3 3 SCN5A - -
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