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217090
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PLASMINOGEN DEFICIENCY, TYPE I
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Respiratory Tract Diseases
Bronchial Diseases
Respiration Disorders
Respiratory Insufficiency
Airway Obstruction
Respiratory Tract Infections
Tracheitis
Tracheal Diseases
Tracheitis
Otorhinolaryngologic Diseases
Ear Diseases
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Dandy-Walker Syndrome
Cerebrovascular Disorders
Intracranial Embolism and Thrombosis
Hydrocephalus
Dandy-Walker Syndrome
Intracranial Hypertension
Hydrocephalus
Dandy-Walker Syndrome
Nervous System Malformations
Dandy-Walker Syndrome
Eye Diseases
Conjunctival Diseases
Conjunctivitis
Corneal Diseases
Eye Injuries
Cardiovascular Diseases
Vascular Diseases
Cerebrovascular Disorders
Intracranial Embolism and Thrombosis
Embolism and Thrombosis
Thromboembolism
Intracranial Embolism and Thrombosis
Thrombosis
Thromboembolism
Intracranial Embolism and Thrombosis
Venous Thrombosis
Thrombophlebitis
Peripheral Vascular Diseases
Phlebitis
Thrombophlebitis
Vasculitis
Phlebitis
Thrombophlebitis
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Afibrinogenemia
Factor XII Deficiency
Coagulation Protein Disorders
Afibrinogenemia
Factor XII Deficiency
Hemorrhagic Disorders
Afibrinogenemia
Factor XII Deficiency
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Dandy-Walker Syndrome
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Afibrinogenemia
Factor XII Deficiency
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Recurrence
Wounds and Injuries
Craniocerebral Trauma
Facial Injuries
Eye Injuries
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