TCMD00134 |
Absence Epilepsy |
DisGeNET |
TCMD00209 |
Acquired Camptodactyly |
DisGeNET |
TCMD01092 |
Akinetic Petit Mal |
CTD;MalaCards;DisGeNET |
TCMD01942 |
Arthrogryposis |
CTD;DisGeNET |
TCMD01943 |
Arthrogryposis Multiplex Congenita 1, Neurogenic, with Myelin Defect |
MalaCards |