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Diseases
Genes (1102)
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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
FMR1
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Fragile X Syndrome
Disinhibition
TTPA
Familial Isolated Vitamin E Deficiency
SERPINE1
Phlebothrombosis
Plasminogen Activator Inhibitor-1 Deficiency
Airway Obstruction
Chronic Periodontitis
MED12
Fg Syndrome
Fragile X Syndrome
SLC17A5
Salla Disease
FECH
Erythropoietic Protoporphyria
PTGS2
Fibrous Dysplasia Of Bone
Pericardial Effusion
Subacromial Bursitis
Hemopericardium
Chronic Periodontitis
EPO
Cardiogenic Shock
Phlebothrombosis
Salla Disease
TFPI
Phlebothrombosis
Airway Obstruction
MMP9
Phlebothrombosis
Pericardial Effusion
Paresis
Airway Obstruction
Fragile X Syndrome
Chronic Periodontitis
BCHE
Toxic Encephalopathy
Paresis
F2
Phlebothrombosis
APP
Salla Disease
Aphasia
Fragile X Syndrome
Disinhibition
IL10
Phlebothrombosis
Pericardial Effusion
Toxic Encephalopathy
Paresis
Fragile X-Associated Tremor/ataxia Syndrome
Airway Obstruction
Chronic Periodontitis
CD55
Protein Losing Enteropathy
F5
Phlebothrombosis
F7
Phlebothrombosis
CYP7B1
Spastic Paraplegia 5a, Autosomal Recessive
HLA-DQB1
Non-Histaminic Angioedema
Paresis
Aphasia