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Diseases
Genes (713)
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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
Spinal Cord Compression
Middle Cerebral Artery Syndrome
Pericardial Effusion
Cystinosis
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
PDGFRB
Primary Familial Brain Calcification
Middle Cerebral Artery Syndrome
EPO
Cardiogenic Shock
Phlebothrombosis
Spinal Cord Compression
PQBP1
Renpenning's Syndrome
SLC20A2
Cyclopia
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
MMP9
Phlebothrombosis
Paresis
Airway Obstruction
Spinal Cord Compression
Middle Cerebral Artery Syndrome
Pericardial Effusion
IL1B
Phlebothrombosis
Renpenning's Syndrome
Middle Cerebral Artery Syndrome
Pericardial Effusion
Cystinosis
IL6
Spinal Cord Compression
Familial Isolated Vitamin E Deficiency
Middle Cerebral Artery Syndrome
Pericardial Effusion
IFIH1
Singleton Merten Syndrome
ADAM10
Alzheimer Disease 18
MTHFR
Phlebothrombosis
Familial Isolated Vitamin E Deficiency
Thrombophilia Due To Thrombin Defect
TFPI
Phlebothrombosis
Airway Obstruction
F13A1
Phlebothrombosis
Thrombophilia Due To Thrombin Defect
PDGFB
Primary Familial Brain Calcification
Paresis
SOD2
Cardiogenic Shock
Middle Cerebral Artery Syndrome