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Diseases
Genes (1750)
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ASL
Liver Failure
Argininosuccinic Aciduria
APOB
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
LIPA
Liver Failure
Acid Lipase Disease
Squamous-Cell Carcinoma Of The Lung
Hypercholesterolemia
TTPA
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
PMM2
Pmm2 Deficiency
TNFAIP3
Haploinsufficiency Of A20
Acute Liver Failure
TNF
Acute Liver Failure
Liver Failure
Squamous-Cell Carcinoma Of The Lung
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Hypercholesterolemia
Hyperuricemia
LDLR
Hypercholesterolemia
Cystinosis
MED12
Squamous-Cell Carcinoma Of The Lung
Fg Syndrome
ABCC9
Cantú Syndrome
PQBP1
Renpenning's Syndrome
MYLK
Hypercholesterolemia
Berdon Syndrome
ASS1
Liver Failure
Argininosuccinic Aciduria
Citrullinemia Type I
FAM20A
Enamel-Renal Syndrome
APOE
Hypercholesterolemia
Hyperuricemia
UBE3B
Kaufman Oculocerebrofacial Syndrome
RHBDF2
Howel–evans Syndrome
KCNJ8
Cantú Syndrome
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
PCSK9
Hypercholesterolemia