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C18. Nutritional and Metabolic Diseases: Metabolic Diseases [MESH:D008659] > Metabolism, Inborn Errors [MESH:D008661] > Amyloidosis, Familial [MESH:D028226] > Cerebral Amyloid Angiopathy, Familial [MESH:D028243] > Cerebral Amyloid Angiopathy, App-Related [MESH:C567787]
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C10. Nervous System Diseases 
C10. Nervous System Diseases
 Nervous System Diseases [MESH:D009422] (13325) 
 Central Nervous System Diseases [MESH:D002493] (9745) 
 Spinal Cord Diseases [MESH:D013118] (4376)
 Brain Diseases [MESH:D001927] (9294) 
 Brain Diseases, Metabolic [MESH:D001928] (3351) 
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Cerebrovascular Disorders [MESH:D002561] (5542) 
 Cerebral Small Vessel Diseases [MESH:D059345] (1292) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Arterial Diseases [MESH:D020765] (2463) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Cerebral Amyloid Angiopathy [MESH:D016657] (470) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Dementia [MESH:D003704] (4498) 
 Alzheimer Disease [MESH:D000544] (4275)
 Neurodegenerative Diseases [MESH:D019636] (6613) 
 Tauopathies [MESH:D024801] (4289) 
 Alzheimer Disease [MESH:D000544] (4275)
 Neurologic Manifestations [MESH:D009461] (8964) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Paralysis [MESH:D010243] (2043)
 Neurobehavioral Manifestations [MESH:D019954] (5230) 
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Intellectual Disability [MESH:D008607] (3054) 
 Mental Retardation, X-Linked [MESH:D038901] (1854) 
 Fragile X Syndrome [MESH:D005600] (353)
C14. Cardiovascular Diseases 
C14. Cardiovascular Diseases
 Cardiovascular Diseases [MESH:D002318] (10123) 
 Vascular Diseases [MESH:D014652] (8691) 
 Cerebrovascular Disorders [MESH:D002561] (5541) 
 Cerebral Small Vessel Diseases [MESH:D059345] (1292) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Arterial Diseases [MESH:D020765] (2468) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Cerebral Amyloid Angiopathy [MESH:D016657] (470) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities 
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
 Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152) 
 Congenital Abnormalities [MESH:D000013] (8109) 
 Chromosome Disorders [MESH:D025063] (2030) 
 Sex Chromosome Disorders [MESH:D025064] (479) 
 Fragile X Syndrome [MESH:D005600] (353)
 Genetic Diseases, Inborn [MESH:D030342] (9766) 
 Chromosome Disorders [MESH:D025063] (2030) 
 Sex Chromosome Disorders [MESH:D025064] (479) 
 Fragile X Syndrome [MESH:D005600] (353)
 Genetic Diseases, X-Linked [MESH:D040181] (3028) 
 Mental Retardation, X-Linked [MESH:D038901] (1867) 
 Fragile X Syndrome [MESH:D005600] (353)
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465) 
 Mental Retardation, X-Linked [MESH:D038901] (1848) 
 Fragile X Syndrome [MESH:D005600] (353)
 Metabolism, Inborn Errors [MESH:D008661] (6032) 
 Amyloidosis, Familial [MESH:D028226] (696) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
C18. Nutritional and Metabolic Diseases 
C18. Nutritional and Metabolic Diseases
 Metabolic Diseases [MESH:D008659] (9025) 
 Brain Diseases, Metabolic [MESH:D001928] (3350) 
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Metabolism, Inborn Errors [MESH:D008661] (6028) 
 Amyloidosis, Familial [MESH:D028226] (696) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Proteostasis Deficiencies [MESH:D057165] (3522) 
 Amyloidosis [MESH:D000686] (791) 
 Amyloidosis, Familial [MESH:D028226] (696) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Cerebral Amyloid Angiopathy [MESH:D016657] (470) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
C22. Animal Diseases 
C22. Animal Diseases
 Animal Diseases [MESH:D000820] (3656) 
 Disease Models, Animal [MESH:D004195] (2058)
C23. Pathological Conditions, Signs and Symptoms 
C23. Pathological Conditions, Signs and Symptoms
 Pathological Conditions, Anatomical [MESH:D020763] (6074) 
 Plaque, Amyloid [MESH:D058225] (334)
 Pathologic Processes [MESH:D010335] (9863) 
 Necrosis [MESH:D009336] (4019)
 Nerve Degeneration [MESH:D009410] (4061)
 Hemorrhage [MESH:D006470] (4451) 
 Intracranial Hemorrhages [MESH:D020300] (3241) 
 Cerebral Hemorrhage [MESH:D002543] (2872) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Inflammation [MESH:D007249] (5241) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Signs and Symptoms [MESH:D012816] (10659) 
 Body Weight [MESH:D001835] (4972) 
 Body Weight Changes [MESH:D001836] (3206) 
 Weight Gain [MESH:D015430] (2595)
 Neurologic Manifestations [MESH:D009461] (8702) 
 Paralysis [MESH:D010243] (2298)
 Neurobehavioral Manifestations [MESH:D019954] (4706) 
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
D02. Organic Chemicals 
D02. Organic Chemicals
 Organic Chemicals [MESH:D009930] (75987) 
 Amines [MESH:D000588] (7350) 
 Polyamines [MESH:D011073] (1133) 
 Diamines [MESH:D003959] (631) 
 Ethylenediamines [MESH:D005029] (322) 
 Edetic Acid [MESH:D004492] (106)
 Carboxylic Acids [MESH:D002264] (13103) 
 Acids, Acyclic [MESH:D000144] (7142) 
 Acetates [MESH:D000085] (1456) 
 Edetic Acid [MESH:D004492] (106)