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Diseases
Genes (753)
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TTPA
Familial Isolated Vitamin E Deficiency
BLM
Bloom Syndrome
BRAF
Acral Myxoinflammatory Fibroblastic Sarcoma
Langerhans Cell Histiocytosis
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
TMC6
Epidermodysplasia Verruciformis
PDGFRB
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
IFIH1
Japanese Encephalitis
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
TMC8
Epidermodysplasia Verruciformis
PDGFB
Primary Familial Brain Calcification
Langerhans Cell Histiocytosis
MYH11
Berdon Syndrome
ASS1
Citrullinemia Type I
MYLK
Berdon Syndrome
TNF
Japanese Encephalitis
Langerhans Cell Histiocytosis
Pleural Effusion
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Bloom Syndrome
Epidermodysplasia Verruciformis
MEN1
Glucagonoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
ITGB3
Japanese Encephalitis
Coronary Thrombosis
Bloom Syndrome
DDX58
Japanese Encephalitis
Singleton Merten Syndrome