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Diseases
Genes (1769)
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MAGEL2
Prader–willi Syndrome
ABCB1
Synovial Sarcoma
Epilepsy
Monosomy
Chromosomal Translocation
PNP
Purine Nucleoside Phosphorylase Deficiency
SNRPN
Prader–willi Syndrome
Microdeletion Syndrome
SCN8A
Epilepsy
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
SS18
Synovial Sarcoma
NDN
Prader–willi Syndrome
GRIN2B
Epilepsy
HDAC4
Epilepsy
2q37 Monosomy
SLC12A5
Epilepsy
PCDH19
Epilepsy
SLC6A1
Epilepsy
GABRB3
Prader–willi Syndrome
Epilepsy
CACNA2D2
Epilepsy
SCN1A
Epilepsy
SCN2A
Epilepsy
BCL2
Synovial Sarcoma
Epilepsy
UBE3A
Prader–willi Syndrome
Epilepsy