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Diseases
Genes (2022)
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APOB
Hypercholesterolemia
Familial Isolated Vitamin E Deficiency
LIPC
High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 12
Hypercholesterolemia
TTPA
Hypercholesterolemia
Familial Isolated Vitamin E Deficiency
LDLR
Myotonic Dystrophy
Hypercholesterolemia
Aortic Aneurysm, Familial Abdominal, 3
FOXP3
Hypercholesterolemia
Aortic Aneurysm, Familial Abdominal, 3
Haemophilia A
Ipex Syndrome
NF2
Neurofibromatosis
Meningioma
F8
Haemophilia A
UMOD
Medullary Cystic Kidney Disease
Hyperuricemia
COL6A1
Bethlem Myopathy
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
EPHA2
Cataract 6, Multiple Types
APOE
Myotonic Dystrophy
Hypercholesterolemia
Hyperuricemia
Aortic Aneurysm, Familial Abdominal, 3
Meningioma
Cadasil
MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
ABCC9
Cantú Syndrome
FECH
Erythropoietic Protoporphyria
COL6A3
Bethlem Myopathy
COL6A2
Bethlem Myopathy
RHBDF2
Howel–evans Syndrome
Meningioma
ABCG2
Erythropoietic Protoporphyria
Hypercholesterolemia
Hyperuricemia
PCSK9
Hypercholesterolemia
Aortic Aneurysm, Familial Abdominal, 3