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Diseases
Genes (985)
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TTPA
Heart Arrhythmia
Familial Isolated Vitamin E Deficiency
EFHC1
Juvenile Myoclonic Epilepsy
ATRX
Thalassemia
Alpha-Thalassemia Mental Retardation Syndrome
F12
Factor Xii Deficiency
PQBP1
Renpenning's Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
RHBDF2
Howel–evans Syndrome
GABRA1
Juvenile Myoclonic Epilepsy
GJA1
Heart Arrhythmia
IFIH1
Singleton Merten Syndrome
CD55
Protein Losing Enteropathy
CACNB4
Juvenile Myoclonic Epilepsy
JRK
Juvenile Myoclonic Epilepsy
CTNS
Cystinosis
OPRK1
Heart Arrhythmia
KCNH2
Heart Arrhythmia
PTPN22
Giant Cell Arteritis
Heart Arrhythmia
MEN1
Alpha-Thalassemia Mental Retardation Syndrome
Glucagonoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
GFI1B
Platelet Storage Pool Deficiency