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Diseases
Genes (488)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
FUS
Myxoid Liposarcoma
Disinhibition
IFIH1
Singleton Merten Syndrome
DDIT3
Myxoid Liposarcoma
CD55
Protein Losing Enteropathy
ALAD
Lead Poisoning
PMP22
Guillain-Barré Syndrome
Guillain-Barré Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MMP9
Guillain-Barré Syndrome
Guillain-Barré Syndrome
Lead Poisoning
BMI1
Accelerated Phase Chronic Myelogenous Leukemia
VDR
Lead Poisoning
DDX58
Singleton Merten Syndrome
HFE
Lead Poisoning
XRCC3
Lead Poisoning
XPO5
Lead Poisoning
MT4
Lead Poisoning
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
CD86
Guillain-Barré Syndrome
Guillain-Barré Syndrome