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Diseases
Genes (189)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
CD55
Protein Losing Enteropathy
SYCP3
Spermatogenesis Arrest
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
KDM3B
Metal Toxicity
DDX58
Singleton Merten Syndrome
FH
Fumarase Deficiency
PTPN22
Giant Cell Arteritis
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
PTEN
Thrombophlebitis
Protein Losing Enteropathy
ITM2B
Cerebral Amyloid Angiopathy
NDP
Vascular Tumor
Uterine Rupture
DICER1
Pinealoblastoma
HLA-DRB1
Macrophagic Myofasciitis
Giant Cell Arteritis
GNAS
Fibrous Dysplasia Of Bone
PLVAP
Protein Losing Enteropathy