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Diseases
Genes (2168)
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EIF2AK3
Wolcott–rallison Syndrome
FANCC
Hyperinsulinemia
Fanconi Anemia, Complementation Group S
FANCA
Hyperinsulinemia
Fanconi Anemia, Complementation Group S
TNF
Hyperinsulinemia
Thyroid Cancer, Nonmedullary, 1
Adult-Onset Still's Disease
Fanconi Anemia, Complementation Group S
TG
Thyroid Dyshormonogenesis 3
Autoimmune Thyroid Disease, Susceptibility To, 3
Thyroid Cancer, Nonmedullary, 1
LIPC
Hyperinsulinemia
Hyperlipidemia Due To Hepatic Triacylglycerol Lipase Deficiency
BRAF
Thyroid Cancer, Nonmedullary, 1
LEP
Hyperinsulinemia
Thyroid Cancer, Nonmedullary, 1
Adiponectin, Serum Level Of, Quantitative Trait Locus 1
CHRNG
Multiple Pterygium Syndrome, Escobar Variant
FAM111B
Hereditary Fibrosing Poikiloderma With Tendon Contractures, Myopathy, And Pulmonary Fibrosis
HOXD13
Brachydactyly Type D
Thyroid Cancer, Nonmedullary, 1
ACY1
Aminoacylase 1 Deficiency
NKX2-1
Thyroid Cancer, Nonmedullary, 1
ADIPOQ
Hyperinsulinemia
Adiponectin, Serum Level Of, Quantitative Trait Locus 1
FANCG
Fanconi Anemia, Complementation Group S
BRIP1
Fanconi Anemia, Complementation Group S
FANCM
Fanconi Anemia, Complementation Group S
FANCD2
Fanconi Anemia, Complementation Group S
SLX4
Fanconi Anemia, Complementation Group S
FANCL
Fanconi Anemia, Complementation Group S