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Diseases
Genes (277)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
DDX58
Hepatitis E
Singleton Merten Syndrome
KDM3B
Metal Toxicity
GABRA5
Social (Pragmatic) Communication Disorder
PTEN
Social (Pragmatic) Communication Disorder
Thrombophlebitis
Protein Losing Enteropathy
FH
Fumarase Deficiency
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
NF1
Fibrous Dysplasia Of Bone
Neurofibromatosis
NF2
Neurofibromatosis
ITM2B
Cerebral Amyloid Angiopathy
NDP
Vascular Tumor
Uterine Rupture
DICER1
Pinealoblastoma
PLVAP
Protein Losing Enteropathy
DGAT1
Protein Losing Enteropathy