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Diseases
Genes (578)
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TTPA
Familial Isolated Vitamin E Deficiency
SCN5A
Cardiac Conduction Defect
PAH
Phenylketonuria (Pku)
PQBP1
Renpenning's Syndrome
FLVCR2
Fowler's Syndrome
IFIH1
Singleton Merten Syndrome
ARG1
Silicosis
PTEN
Silicosis
Thrombophlebitis
Protein Losing Enteropathy
Salmonella Infection
CD55
Protein Losing Enteropathy
IL1B
Silicosis
Toxoplasmosis
Salmonella Infection
Irritant Contact Dermatitis
Renpenning's Syndrome
TNF
Silicosis
Toxoplasmosis
Salmonella Infection
Irritant Contact Dermatitis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
IL6
Fibrous Dysplasia Of Bone
Silicosis
Toxoplasmosis
Aseptic Meningitis
Irritant Contact Dermatitis
Familial Isolated Vitamin E Deficiency
RB1
Pinealoblastoma
Trilateral Retinoblastoma
STAT6
Hemangiopericytoma
NAB2
Hemangiopericytoma
CCL2
Silicosis
Toxoplasmosis
QDPR
Phenylketonuria (Pku)
CPM
Silicosis
NOS2
Silicosis
PDZRN4
Silicosis