Kardiogenetik
Kardiogenetik
| Erkrankung | Gen | OMIM |
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|
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| Brugada Syndrom | SCN5A | 601144 |
| Dilatative Kardiomyopathie |
MYBPC3, MYH7, LMNA, TNNT2, SCN5A, LDB3, PLN, ACTN2, VCL, SGCD, CSRP3, DES, TNNI3, TPM1 |
115200 |
| Familiäre hypertrophe Kardiomyopathie | MYBPC3, MYH7, TNNT2, TNNI3, TPM1, MYL2, MYL3, CAV3, CSRP3, VCL | 192600 |
| Jervell-Lange-Nielsen Syndrom | KCNQ1, KCNE1 | 220400 |
| Long-QT Syndrom | KCNQ1, KCNH2, KCNE1, KCNE2, SCN5A | 192500 |
| Mikrodeletionssyndrom 22q11.2 | - | 192430 |
| Noonan Syndrom 1 | PTPN11 | 163950 |
| Noonan Syndrom 4 | SOS1 | 610733 |
| Romano-Ward Syndrom | KCNQ1, KCNH2, KCNE1, KCNE2, SCN5A | 192500 |