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Diseases
Genes (473)
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ASL
Argininosuccinic Aciduria
ATP7B
Wilson's Disease
PMM2
Pmm2 Deficiency
IFIH1
Singleton Merten Syndrome
DMPK
Myotonic Dystrophy
ANXA5
Wilson's Disease
CNBP
Myotonic Dystrophy
RB1
Pinealoblastoma
Wilson's Disease
Trilateral Retinoblastoma
CP
Wilson's Disease
MED12
Phyllodes Tumor
APOE
Myotonic Dystrophy
Wilson's Disease
TNF
Myotonic Dystrophy
Wilson's Disease
Cardiac Tamponade
IL6
Myotonic Dystrophy
Argininosuccinic Aciduria
Wilson's Disease
PRNP
Myotonic Dystrophy
Wilson's Disease
KDM3B
Metal Toxicity
AHCY
Pmm2 Deficiency
Wilson's Disease
ASMT
Pinealoblastoma
Wilson's Disease
NKX2-5
Myotonic Dystrophy
DDX58
Singleton Merten Syndrome
LOX
Wilson's Disease