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 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.300 Cerebrovascular Disorders .
C10.228.140.300.510 Intracranial Arterial Diseases .
C10.228.140.300.510.200 Cerebral Arterial Diseases .
C10.228.140.300.510.200.200 Cerebral Amyloid Angiopathy .
C14 Cardiovascular Diseases .
C14.907 Vascular Diseases .
C14.907.077 Angiomatosis .
C14.907.077.410 Klippel-Trenaunay-Weber Syndrome .
C14.907.253 Cerebrovascular Disorders .
C14.907.253.560 Intracranial Arterial Diseases .
C14.907.253.560.200 Cerebral Arterial Diseases .
C14.907.253.560.200.200 Cerebral Amyloid Angiopathy .
C14.907.320 Diabetic Angiopathies .
C14.907.617 Peripheral Vascular Diseases .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.100 Blood Coagulation Disorders .
C15.378.100.100 Blood Coagulation Disorders, Inherited .
C15.378.100.100.900 von Willebrand Diseases .
C15.378.100.141 Coagulation Protein Disorders .
C15.378.100.141.900 von Willebrand Diseases .
C15.378.140 Blood Platelet Disorders .
C15.378.140.900 von Willebrand Diseases .
C15.378.463 Hemorrhagic Disorders .
C15.378.463.920 von Willebrand Diseases .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.099 Blood Coagulation Disorders, Inherited .
C16.320.099.920 von Willebrand Diseases .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.845 Proteostasis Deficiencies .
C18.452.845.500 Amyloidosis .
C18.452.845.500.100 Cerebral Amyloid Angiopathy .
C19 Endocrine System Diseases .
C19.246 Diabetes Mellitus .
C19.246.099 Diabetes Complications .
C19.246.099.500 Diabetic Angiopathies .
 Synonyms & Historicals
Cerebral Amyloid Angiopathy .
Angiopathy, Cerebral Amyloid .
Angiopathy, Congophilic .
Cerebral Amyloid Angiopathies .
Congophilic Angiopathies .
Amyloid Angiopathy, Cerebral .
Congophilic Angiopathy .
Sporadic Cerebral Amyloid Angiopathy .
A heterogeneous group of sporadic or familial disorders characterized by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES. Clinical features include multiple, small lobar CEREBRAL HEMORRHAGE; cerebral ischemia (BRAIN ISCHEMIA); and CEREBRAL INFARCTION. Cerebral amyloid angiopathy is unrelated to generalized AMYLOIDOSIS. Amyloidogenic peptides in this condition are nearly always the same ones found in ALZHEIMER DISEASE. (from Kumar: Robbins and Cotran: Pathologic Basis of Disease, 7th ed., 2005) .
Klippel-Trenaunay-Weber Syndrome .
Angio-Osteohypertrophy Syndrome .
Angioosteohypertrophy Syndrome .
Congenital Dysplastic Angiopathy .
KTW Syndrome .
Klippel Trenaunay Syndrome .
Klippel-Trenaunay Syndrome .
Klippel-Trénaunay-Weber Syndrome .
Angio Osteohypertrophy Syndrome .
Angio-Osteohypertrophy Syndromes .
Angioosteohypertrophy Syndromes .
Angiopathies, Congenital Dysplastic .
Angiopathy, Congenital Dysplastic .
Congenital Dysplastic Angiopathies .
Disease, Klippel-Trenaunay .
Dysplastic Angiopathies, Congenital .
Dysplastic Angiopathy, Congenital .
KTW Syndromes .
Klippel Trenaunay Disease .
Klippel Trenaunay Weber Syndrome .
Klippel Trénaunay Weber Syndrome .
Klippel-Trenaunay Syndromes .
Syndrome, Angio-Osteohypertrophy .
Syndrome, Angioosteohypertrophy .
Syndrome, KTW .
Syndrome, Klippel Trenaunay .
Syndrome, Klippel-Trenaunay .
Syndrome, Klippel-Trenaunay-Weber .
Syndrome, Klippel-Trénaunay-Weber .
Syndromes, Angio-Osteohypertrophy .
Syndromes, Angioosteohypertrophy .
Syndromes, KTW .
Syndromes, Klippel-Trenaunay .
Klippel-Trenaunay Disease .
A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA), venous malformations (ARTERIOVENOUS FISTULA), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator. .
Diabetic Angiopathies .
Angiopathies, Diabetic .
Angiopathy, Diabetic .
Diabetic Angiopathy .
Diabetic Microangiopathies .
Diabetic Microangiopathy .
Diabetic Vascular Complication .
Diabetic Vascular Disease .
Microangiopathies, Diabetic .
Vascular Complication, Diabetic .
Vascular Complications, Diabetic .
Vascular Disease, Diabetic .
Vascular Diseases, Diabetic .
Diabetic Vascular Complications .
Diabetic Vascular Diseases .
Microangiopathy, Diabetic .
von Willebrand Diseases .
Vascular Pseudohemophilia .
Von Willebrand Disorder .
Von Willebrand's Factor Deficiency .
von Willebrand Disease, Recessive Form .
von Willebrand's Disease .
von Willebrand's Diseases .
Angiohemophilias .
Disorder, Von Willebrand .
Pseudohemophilia, Vascular .
Pseudohemophilias, Vascular .
Vascular Hemophilia .
Vascular Hemophilias .
Vascular Pseudohemophilias .
Angiohemophilia .
Hemophilia, Vascular .
von Willebrand Disease .
Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion. .
Peripheral Vascular Diseases .
Diseases, Peripheral Vascular .
Angiopathies, Peripheral .
Angiopathy, Peripheral .
Disease, Peripheral Vascular .
Peripheral Angiopathy .
Peripheral Vascular Disease .
Vascular Disease, Peripheral .
Peripheral Angiopathies .
Vascular Diseases, Peripheral .
Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. .