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Diseases
Genes (1195)
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APOB
Familial Isolated Vitamin E Deficiency
Insulin Resistance
Tauopathy
Hypercholesterolemia
TTPA
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
ASL
Argininosuccinic Aciduria
LIPA
Insulin Resistance
Acid Lipase Disease
Hypercholesterolemia
PYGM
Glycogen Storage Disease Type V
FOXP3
Ipex Syndrome
Hypercholesterolemia
WRN
Werner Syndrome
PMM2
Pmm2 Deficiency
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
Fg Syndrome
LDLR
Cystinosis
Hypercholesterolemia
GNAQ
Erdheim–chester Disease
Sturge–weber Syndrome
Hypercholesterolemia
UMOD
Medullary Cystic Kidney Disease
SLC17A5
Salla Disease
Hypercholesterolemia
MED12
Fg Syndrome
NGLY1
Ngly1 Deficiency
APOE
Fragile X-Associated Tremor/ataxia Syndrome
Tauopathy
Hypercholesterolemia
RHBDF2
Howel–evans Syndrome
LIPC
Hypercholesterolemia
Large For Gestational Age
LPL
Insulin Resistance
Hypercholesterolemia
NT5C2
Autosomal Recessive Spastic Paraplegia Type 45