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Diseases
Genes (924)
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APOB
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
TTPA
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
ASL
Argininosuccinic Aciduria
LIPA
Acid Lipase Disease
Hypercholesterolemia
PMM2
Pmm2 Deficiency
LDLR
Hypercholesterolemia
Cystinosis
ABCC9
Cantú Syndrome
PQBP1
Renpenning's Syndrome
MYLK
Hypercholesterolemia
Berdon Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
APOE
Hypercholesterolemia
Hyperuricemia
UBE3B
Kaufman Oculocerebrofacial Syndrome
RHBDF2
Howel–evans Syndrome
KCNJ8
Cantú Syndrome
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
PCSK9
Hypercholesterolemia
CYP7A1
Hypercholesterolemia
APOA1
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
Hyperuricemia