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Diseases
Genes (163)
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ASL
Argininosuccinic Aciduria
Hyperoxia
TTPA
Familial Isolated Vitamin E Deficiency
Hyperoxia
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
CYP1A1
Hyperoxia
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
KDM3B
Metal Toxicity
DDX58
Singleton Merten Syndrome
FH
Fumarase Deficiency
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
TNFRSF1A
Hyperoxia
AHR
Hyperoxia
ASS1
Argininosuccinic Aciduria
Hyperoxia
IL6
Argininosuccinic Aciduria
Familial Isolated Vitamin E Deficiency
Hyperoxia
CDKN1A
Hyperoxia
NOS3
Familial Isolated Vitamin E Deficiency
Hyperoxia
CDK4
Hyperoxia
Vascular Tumor