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Prader-willi syndrome

Disease Term Disease ID Gene Symbol References

Prader-Willi Syndrome C0032897
IPW
NDN
SNRPN 8723064
MKRN3
HERC2
MKRN3-AS1
NPAP1
MAGEL2 29588991, 24076603
MRAP2 26795956
PWAR1
SNORD115-1
PWRN1
SNORD116-1
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1 177901
SNRPN
MAGEL2
NDN
OCA2
SNORD116@
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2 177904
SNRPN
MAGEL2
NDN
OCA2
SNORD116@
Prader-Willi syndrome due to translocation 177907
SNRPN
Prader-Willi syndrome due to imprinting mutation 177910
SNRPN
MAGEL2
NDN
SNORD116@
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 98754
SNRPN
MAGEL2
NDN
OCA2

 

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