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Diseases
Genes (519)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
FAM20A
Enamel-Renal Syndrome
IFIH1
Valvular Heart Disease
Singleton Merten Syndrome
Polymyositis
TNF
Valvular Heart Disease
Hypopigmentation
Polymyositis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
IL1B
Valvular Heart Disease
Polymyositis
Renpenning's Syndrome
Erdheim–chester Disease
AGGF1
Klippel-Trenaunay-Weber Syndrome
HTR2B
Valvular Heart Disease
ASS1
Citrullinemia Type I
EPG5
Hypopigmentation
RB1
Pinealoblastoma
Trilateral Retinoblastoma
GALE
Galactose-1-Phosphate Uridylyltransferase Deficiency
GALK1
Galactose-1-Phosphate Uridylyltransferase Deficiency
BRAF
Erdheim–chester Disease
FGFR1
Valvular Heart Disease
CCL2
Valvular Heart Disease
Polymyositis
TIMP1
Valvular Heart Disease
Polymyositis
IL18
Valvular Heart Disease
Polymyositis
CASP3
Valvular Heart Disease
Galactose-1-Phosphate Uridylyltransferase Deficiency