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Diseases
Genes (1681)
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SALL4
Heart Arrhythmia
Holt–oram Syndrome
Duane-Radial Ray Syndrome
TTPA
Heart Arrhythmia
Familial Isolated Vitamin E Deficiency
TBX5
Heart Arrhythmia
Holt–oram Syndrome
SLC6A19
Hartnup Disease
PYGM
Glycogen Storage Disease Type V
SGCE
Myoclonic Dystonia
ITGB3
Glanzmann's Thrombasthenia
TGFBR1
Uterine Rupture
Loeys–dietz Syndrome
TGFBR2
Uterine Rupture
Loeys–dietz Syndrome
FECH
Erythropoietic Protoporphyria
PQBP1
Renpenning's Syndrome
ITGA2B
Glanzmann's Thrombasthenia
PRPS1
Arts Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
Chronic Periodontitis
ACE
Heart Arrhythmia
Chronic Periodontitis
Glycogen Storage Disease Type V
NPM1
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia
GJA1
Heart Arrhythmia
PRKAR1A
Fibrous Dysplasia Of Bone
Acute Promyelocytic Leukemia
Enamel-Renal Syndrome