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Diseases
Genes (375)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
KDR
Hemangioma
Infantile Hemangioma
FLT4
Hemangioma
Infantile Hemangioma
ANTXR1
Hemangioma
Infantile Hemangioma
IFIH1
Singleton Merten Syndrome
PTEN
Hemangioma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
IDH1
Hemangioma
IDH2
Hemangioma
KDM3B
Metal Toxicity
DDX58
Singleton Merten Syndrome
YAP1
Hemangioma
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
PTPN22
Giant Cell Arteritis
ITM2B
Cerebral Amyloid Angiopathy