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Diseases
Genes (846)
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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
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
IFIH1
Japanese Encephalitis
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
PDGFB
Callosity
Primary Familial Brain Calcification
Langerhans Cell Histiocytosis
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
TNF
Callosity
Japanese Encephalitis
Pleural Effusion
Langerhans Cell Histiocytosis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Bloom Syndrome
MEN1
Glucagonoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
ITGB3
Japanese Encephalitis
Coronary Thrombosis
Bloom Syndrome
DDX58
Japanese Encephalitis
Singleton Merten Syndrome
UNG
Bloom Syndrome
PLAT
Coronary Thrombosis
Bloom Syndrome