TCMD05842 |
Corneal Dystrophy, Posterior Polymorphous, 1 |
MalaCards |
TCMD05965 |
COWDEN SYNDROME 7 |
MalaCards;DisGeNET |
TCMD06316 |
Deficiency of mevalonate kinase |
DisGeNET |
TCMD06354 |
DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA |
MalaCards;DisGeNET |
TCMD06597 |
Developmental and Epileptic Encephalopathy 50 |
CTD;MalaCards |