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Diseases
Genes (967)
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RAI1
Smith–magenis Syndrome
NDN
Mammary Tumor
Prader–willi Syndrome
MAGEL2
Prader–willi Syndrome
AUTS2
Mental Retardation, Autosomal Dominant 26
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
SNRPN
Prader–willi Syndrome
Microdeletion Syndrome
RHBDF2
Howel–evans Syndrome
KRT17
Pachyonychia Congenita
SS18
Synovial Sarcoma
KRT16
Pachyonychia Congenita
PLG
Ligneous Conjunctivitis
BCL2
Synovial Sarcoma
ERBB2
Synovial Sarcoma
Mammary Tumor
Smith–magenis Syndrome
KRT6A
Pachyonychia Congenita
EGFR
Severe Acute Respiratory Syndrome
Synovial Sarcoma
Mammary Tumor
MKRN3
Prader–willi Syndrome
ACE
Severe Acute Respiratory Syndrome
Synovial Sarcoma
ERF
Chiari Malformation
FUZ
Chiari Malformation