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Diseases
Genes (749)
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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
ARID1B
Coffin-Siris Syndrome 2
TTPA
Familial Isolated Vitamin E Deficiency
ATR
Microcephaly And Chorioretinopathy, Autosomal Recessive, 2
Coffin-Siris Syndrome 2
FLVCR1
Posterior Column Ataxia With Retinitis Pigmentosa
EPO
Cardiogenic Shock
Phlebothrombosis
Spinal Cord Compression
CENPJ
Microcephaly And Chorioretinopathy, Autosomal Recessive, 2
PQBP1
Renpenning's Syndrome
MMP9
Phlebothrombosis
Paresis
Airway Obstruction
Coffin-Siris Syndrome 2
Spinal Cord Compression
Middle Cerebral Artery Syndrome
Pericardial Effusion
FAM20A
Enamel-Renal Syndrome
IL1B
Phlebothrombosis
Renpenning's Syndrome
Middle Cerebral Artery Syndrome
Pericardial Effusion
Cystinosis
ARID1A
Coffin-Siris Syndrome 2
IL6
Spinal Cord Compression
Familial Isolated Vitamin E Deficiency
Middle Cerebral Artery Syndrome
Pericardial Effusion
SMARCB1
Pinealoblastoma
Paresis
Coffin-Siris Syndrome 2
IFIH1
Singleton Merten Syndrome
SMARCE1
Coffin-Siris Syndrome 2
SOX11
Coffin-Siris Syndrome 2