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Diseases
Genes (1510)
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PLAT
Cardiogenic Shock
Cerebral Vasospasm
Phlebothrombosis
Spinal Epidural Hematoma
Non-Histaminic Angioedema
Paresis
Airway Obstruction
Cardiac Tamponade
Spinal Cord Compression
Middle Cerebral Artery Syndrome
Pericardial Effusion
CCL2
Cerebral Vasospasm
Phlebothrombosis
Retinoblastoma
Spinal Cord Compression
Middle Cerebral Artery Syndrome
Pericardial Effusion
Cystinosis
RB1
Pinealoblastoma
Retinoblastoma
Trilateral Retinoblastoma
SERPINE1
Phlebothrombosis
Plasminogen Activator Inhibitor-1 Deficiency
Airway Obstruction
Middle Cerebral Artery Syndrome
F2
Phlebothrombosis
Thrombophilia Due To Thrombin Defect
TTPA
Familial Isolated Vitamin E Deficiency
EPO
Cardiogenic Shock
Phlebothrombosis
Spinal Cord Compression
LMNA
Retinoblastoma
Pericardial Effusion
Limb–girdle Muscular Dystrophy
MMP9
Phlebothrombosis
Paresis
Airway Obstruction
Retinoblastoma
Spinal Cord Compression
Middle Cerebral Artery Syndrome
Pericardial Effusion
Limb–girdle Muscular Dystrophy
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
IL6
Retinoblastoma
Spinal Cord Compression
Familial Isolated Vitamin E Deficiency
Middle Cerebral Artery Syndrome
Pericardial Effusion
FAM20A
Enamel-Renal Syndrome
IL1B
Phlebothrombosis
Retinoblastoma
Renpenning's Syndrome
Middle Cerebral Artery Syndrome
Pericardial Effusion
Cystinosis
UBE3B
Kaufman Oculocerebrofacial Syndrome
MTHFR
Phlebothrombosis
Retinoblastoma
Familial Isolated Vitamin E Deficiency
Thrombophilia Due To Thrombin Defect
IFIH1
Singleton Merten Syndrome
TFPI
Phlebothrombosis
Airway Obstruction
F13A1
Phlebothrombosis
Thrombophilia Due To Thrombin Defect
PLAU
Phlebothrombosis
Retinoblastoma
Middle Cerebral Artery Syndrome