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Diseases
Genes (873)
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PLAT
Cardiogenic Shock
Cerebral Vasospasm
Phlebothrombosis
Spinal Epidural Hematoma
Non-Histaminic Angioedema
Pericardial Effusion
Toxic Encephalopathy
Paresis
Aphasia
Airway Obstruction
Hemopericardium
Cardiac Tamponade
Spinal Cord Compression
Meningoencephalitis
Middle Cerebral Artery Syndrome
CCL2
Cerebral Vasospasm
Phlebothrombosis
Pericardial Effusion
Spinal Cord Compression
Middle Cerebral Artery Syndrome
SERPINE1
Phlebothrombosis
Plasminogen Activator Inhibitor-1 Deficiency
Airway Obstruction
Middle Cerebral Artery Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
FMR1
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Disinhibition
Renpenning's Syndrome
EPO
Cardiogenic Shock
Phlebothrombosis
Salla Disease
Spinal Cord Compression
MED12
Fg Syndrome
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome
MMP9
Phlebothrombosis
Pericardial Effusion
Paresis
Airway Obstruction
Spinal Cord Compression
Middle Cerebral Artery Syndrome
IL6
Familial Isolated Vitamin E Deficiency
Pericardial Effusion
Subacromial Bursitis
Spinal Cord Compression
Meningoencephalitis
Middle Cerebral Artery Syndrome
IL1B
Phlebothrombosis
Pericardial Effusion
Subacromial Bursitis
Renpenning's Syndrome
Middle Cerebral Artery Syndrome
IFIH1
Singleton Merten Syndrome
TFPI
Phlebothrombosis
Airway Obstruction
SOD2
Cardiogenic Shock
Middle Cerebral Artery Syndrome
PTGS2
Pericardial Effusion
Subacromial Bursitis
Hemopericardium
F2
Phlebothrombosis
BCHE
Toxic Encephalopathy
Paresis
PLAU
Phlebothrombosis
Middle Cerebral Artery Syndrome
MTOR
Toxic Encephalopathy
Paresis
Fragile X-Associated Tremor/ataxia Syndrome
Middle Cerebral Artery Syndrome