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Diseases
Genes (1679)
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SCN5A
Enamel-Renal Syndrome
Progressive Familial Heart Block, Type Ia
Progressive Familial Heart Block
Atrioventricular Block
Trifascicular Block
Bundle Branch Block
SALL4
Holt–oram Syndrome
Duane-Radial Ray Syndrome
RB1
Pinealoblastoma
Retinoblastoma
Trilateral Retinoblastoma
TBX5
Retinoblastoma
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
LMNA
Acute Promyelocytic Leukemia
Retinoblastoma
Holt–oram Syndrome
Heart Block
Atrioventricular Block
Second-Degree Atrioventricular Block
TGFBR2
Uterine Rupture
Retinoblastoma
Loeys–dietz Syndrome
TGFBR1
Uterine Rupture
Loeys–dietz Syndrome
PQBP1
Renpenning's Syndrome
ITGA2B
Glanzmann's Thrombasthenia
PRPS1
Arts Syndrome
FAM20A
Enamel-Renal Syndrome
NPM1
Acute Promyelocytic Leukemia
Retinoblastoma
RARA
Acute Promyelocytic Leukemia
Retinoblastoma