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Diseases
Genes (594)
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TTPA
Familial Isolated Vitamin E Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
BRAF
Acral Myxoinflammatory Fibroblastic Sarcoma
Langerhans Cell Histiocytosis
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
IFIH1
Japanese Encephalitis
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
AGGF1
Klippel–trénaunay Syndrome
PAH
Phenylketonuria
ERGIC1
Arthrogryposis
PDGFB
Primary Familial Brain Calcification
Langerhans Cell Histiocytosis
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
MEN1
Glucagonoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
TNF
Diverticulum
Japanese Encephalitis
Pleural Effusion
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Langerhans Cell Histiocytosis
ITGB3
Japanese Encephalitis
Coronary Thrombosis
DDX58
Japanese Encephalitis
Singleton Merten Syndrome
XPR1
Primary Familial Brain Calcification