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Diseases
Genes (539)
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TTPA
Familial Isolated Vitamin E Deficiency
SCN5A
Cardiac Conduction Defect
PQBP1
Renpenning's Syndrome
FLVCR2
Fowler's Syndrome
IFIH1
Singleton Merten Syndrome
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
STAT6
Hemangiopericytoma
NAB2
Hemangiopericytoma
DDX58
Singleton Merten Syndrome
TRPM4
Cardiac Conduction Defect
PTEN
Thrombophlebitis
Cavernous Hemangioma
Protein Losing Enteropathy
Salmonella Infection
FH
Fumarase Deficiency
ADARB2
Prescription Drug Abuse
TTC21B
Prescription Drug Abuse
FAM184A
Prescription Drug Abuse
PCDH15
Prescription Drug Abuse
CDCP1
Prescription Drug Abuse
CSMD1
Prescription Drug Abuse
XYLT1
Prescription Drug Abuse