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Diseases
Genes (202)
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TTPA
Familial Isolated Vitamin E Deficiency
Hyperoxia
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
CD55
Protein Losing Enteropathy
CYP1A1
Hyperoxia
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
KDM3B
Metal Toxicity
DDX58
Singleton Merten Syndrome
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
TNFRSF1A
Hyperoxia
AHR
Hyperoxia
IL6
Fibrous Dysplasia Of Bone
Familial Isolated Vitamin E Deficiency
Hyperoxia
CDK4
Fibrous Dysplasia Of Bone
Hyperoxia
CDKN1A
Hyperoxia
NOS3
Familial Isolated Vitamin E Deficiency
Hyperoxia
PTEN
Thrombophlebitis
Protein Losing Enteropathy
AGER
Hyperoxia
MMP9
Hyperoxia