TCMD17565 |
Osteogenesis Imperfecta, Type Ii |
MalaCards |
TCMD18195 |
Paroxysmal atrial fibrillation |
DisGeNET |
TCMD18869 |
Platelet Disorder, Familial, with Associated Myeloid Malignancy |
MalaCards;DisGeNET |
TCMD20824 |
Romano-Ward Syndrome |
DisGeNET |
TCMD21451 |
Short QT Syndrome 3 |
MalaCards;DisGeNET |