TCMD15629 |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4 |
MalaCards;DisGeNET |
TCMD16212 |
Neonatal encephalopathy |
DisGeNET |
TCMD17003 |
Nonketotic Hyperglycinemia |
DisGeNET |
TCMD19496 |
Profound global developmental delay |
DisGeNET |
TCMD20000 |
Pyruvate Dehydrogenase E1-Alpha Deficiency |
MalaCards |