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Diseases
Genes (931)
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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
FMR1
Fragile X Syndrome
Fg Syndrome
Fragile X-Associated Tremor/ataxia 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
EPO
Cardiogenic Shock
Phlebothrombosis
Salla Disease
Spinal Cord Compression
MED12
Fragile X Syndrome
Fg Syndrome
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
TFPI
Phlebothrombosis
Airway Obstruction
PTGS2
Pericardial Effusion
Subacromial Bursitis
Hemopericardium
BCHE
Toxic Encephalopathy
Paresis
APP
Fragile X Syndrome
Salla Disease
Aphasia
Disinhibition
F2
Phlebothrombosis
F5
Phlebothrombosis
F7
Phlebothrombosis
CYP7B1
Spastic Paraplegia 5a, Autosomal Recessive
HLA-DQB1
Non-Histaminic Angioedema
Paresis
Aphasia
JAK2
Phlebothrombosis