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Diseases
Genes (206)
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ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
SLC6A19
Hartnup Disease
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
ALAD
Lead Poisoning
RB1
Pinealoblastoma
Trilateral Retinoblastoma
VDR
Lead Poisoning
DDX58
Singleton Merten Syndrome
HFE
Lead Poisoning
MMP9
Lead Poisoning
XRCC3
Lead Poisoning
XPO5
Lead Poisoning
MT4
Lead Poisoning
FH
Fumarase Deficiency
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency