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Diseases
Genes (907)
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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
FMR1
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Fragile X Syndrome
Disinhibition
Renpenning's Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
SERPINE1
Phlebothrombosis
Plasminogen Activator Inhibitor-1 Deficiency
Airway Obstruction
CCL2
Cerebral Vasospasm
Phlebothrombosis
Pericardial Effusion
Spinal Cord Compression
COL2A1
Collagen, Type Ii, Alpha-1
EPO
Cardiogenic Shock
Phlebothrombosis
Salla Disease
Spinal Cord Compression
MED12
Fg Syndrome
Fragile X Syndrome
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
TFPI
Phlebothrombosis
Airway Obstruction
PAH
Phenylketonuria
Pericardial Effusion
PTGS2
Pericardial Effusion
Subacromial Bursitis
Hemopericardium
BCHE
Toxic Encephalopathy
Paresis
F2
Phlebothrombosis
APP
Salla Disease
Fragile X Syndrome
Aphasia
Disinhibition
F5
Phlebothrombosis
F7
Phlebothrombosis
HLA-DQB1
Non-Histaminic Angioedema
Paresis
Aphasia