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Diseases
Genes (1186)
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APOB
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
TTPA
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
LIPA
Acid Lipase Disease
Hypercholesterolemia
LDLR
Hypercholesterolemia
Cystinosis
ABCC9
Cantú Syndrome
PQBP1
Renpenning's Syndrome
MYLK
Hypercholesterolemia
Berdon Syndrome
MED12
Fg Syndrome
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
CYP7A1
Hypercholesterolemia
APOA1
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
Hyperuricemia
LPL
Hypercholesterolemia
ACTG2
Berdon Syndrome
FLNA
Vascular Malformation
Intestinal Neuronal Dysplasia
Hypercholesterolemia
Fg Syndrome