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Diseases
Genes (210)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
KDM3B
Metal Toxicity
DDX58
Singleton Merten Syndrome
FH
Fumarase Deficiency
TICAM1
Pneumoconiosis
H3-4
Pneumoconiosis
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
ACAN
Pneumoconiosis
IL4
Pneumoconiosis
HS3ST6
Pneumoconiosis
TMPRSS3
Pneumoconiosis
CDH23
Pneumoconiosis
IL27RA
Pneumoconiosis
PTPRZ1
Pneumoconiosis