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Diseases
Genes (1447)
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APOB
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
TTPA
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
LIPA
Acid Lipase Disease
Hypercholesterolemia
SLC6A19
Hartnup Disease
LDLR
Hypercholesterolemia
Cystinosis
ABCC9
Cantú Syndrome
PQBP1
Renpenning's Syndrome
MYLK
Hypercholesterolemia
Berdon Syndrome
PCSK9
Hypercholesterolemia
Wilms Tumor 3
DICER1
Pinealoblastoma
Wilms Tumor 3
MED12
Fg Syndrome
WT1
Vascular Malformation
Wilms Tumor 3
FAM20A
Enamel-Renal Syndrome
GPC3
Wilms Tumor 3
APOE
Hypercholesterolemia
Hyperuricemia
UBE3B
Kaufman Oculocerebrofacial Syndrome
RHBDF2
Howel–evans Syndrome
KCNJ8
Cantú Syndrome
Enamel-Renal Syndrome