TCMD15231 |
Mitochondrial Dna Depletion Syndrome 12b |
MalaCards |
TCMD15956 |
Myopathy |
MalaCards;DisGeNET |
TCMD18195 |
Paroxysmal atrial fibrillation |
DisGeNET |
TCMD20492 |
Restrictive cardiomyopathy |
CTD;MalaCards;DisGeNET |
TCMD21276 |
Sensorineural Hearing Loss (disorder) |
DisGeNET |