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Diseases
Genes (860)
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TTPA
Familial Isolated Vitamin E Deficiency
SCN5A
Cardiac Conduction Defect
IL6
Fibrous Dysplasia Of Bone
Acute Coronary Syndrome
Toxoplasmosis
Aseptic Meningitis
Irritant Contact Dermatitis
Familial Isolated Vitamin E Deficiency
PAH
Phenylketonuria (Pku)
PQBP1
Renpenning's Syndrome
FLVCR2
Fowler's Syndrome
IFIH1
Singleton Merten Syndrome
TNF
Acute Coronary Syndrome
Toxoplasmosis
Salmonella Infection
Irritant Contact Dermatitis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Vitamin Deficiency
CD55
Protein Losing Enteropathy
CRP
Acute Coronary Syndrome
Phenylketonuria (Pku)
Vitamin Deficiency
TNNI3
Acute Coronary Syndrome
SYCP3
Spermatogenesis Arrest
MMP9
Acute Coronary Syndrome
PAPPA
Acute Coronary Syndrome
TLR4
Acute Coronary Syndrome
Toxoplasmosis
Salmonella Infection
ALB
Acute Coronary Syndrome
Phenylketonuria (Pku)
Protein Losing Enteropathy
Aseptic Meningitis
PON1
Acute Coronary Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma
STAT6
Hemangiopericytoma
NAB2
Hemangiopericytoma