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Diseases
Genes (673)
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TTPA
Familial Isolated Vitamin E Deficiency
BLM
Bloom Syndrome
COL2A1
Collagen, Type Ii, Alpha-1
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
PAH
Phenylketonuria
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
PDGFB
Primary Familial Brain Calcification
MYLK
Berdon Syndrome
MEN1
Glucagonoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
TNF
Diverticulum
Japanese Encephalitis
Pleural Effusion
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Bloom Syndrome
ITGB3
Japanese Encephalitis
Coronary Thrombosis
Bloom Syndrome
DDX58
Japanese Encephalitis
Singleton Merten Syndrome
UNG
Bloom Syndrome