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Diseases
Genes (1309)
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SCN5A
Enamel-Renal Syndrome
Progressive Familial Heart Block, Type Ia
Progressive Familial Heart Block
Atrioventricular Block
Trifascicular Block
SALL4
Holt–oram Syndrome
Duane-Radial Ray Syndrome
TBX5
Holt–oram Syndrome
Atrioventricular Block
ASL
Argininosuccinic Aciduria
SLC6A19
Hartnup Disease
PYGM
Glycogen Storage Disease Type V
TTPA
Familial Isolated Vitamin E Deficiency
SGCE
Myoclonic Dystonia
ITGB3
Glanzmann's Thrombasthenia
PMM2
Pmm2 Deficiency
TGFBR1
Uterine Rupture
Loeys–dietz Syndrome
TGFBR2
Uterine Rupture
Loeys–dietz Syndrome
PQBP1
Renpenning's Syndrome
ITGA2B
Glanzmann's Thrombasthenia
PRPS1
Arts Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
Myasthenia Gravis
LMNA
Acute Promyelocytic Leukemia
Holt–oram Syndrome
Heart Block
Atrioventricular Block
NPM1
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia