Cerebral Amyloid Angiopathy, Familial [cerebrální amyloidová angiopatie, familiární typ]

topical
1
Terms

amyloidová angiopatie islandského typu
amyloidóza VI
cerebrální amyloidní angiopatie, familiární
cerebrální amyloidová angiopatie, familiární forma
cerebrální amyloidová angiopatie, islandský typ
dědičná mozková amyloidní angiopatie
dědičná mozková amyloidní angiopatie, islandský typ
HCHWA
hereditární cerebrální amyloidová angiopatie
hereditární mozkové krvácení s amyloidózou
mozek - angiopatie amyloidní familiární
mozková amyloidní angiopatie, geneticky podmíněná

 

Amyloidosis VI
Amyloidosis, Cerebroarterial, Icelandic Type
Autosomal Dominant Cerebrovascular Amyloidosis
Cerebral Amyloid Angiopathy, Cst3-Related
Cerebral Amyloid Angiopathy, Genetic
Cerebral Amyloid Angiopathy, Hereditary
Cerebral Hemorrhage, Hereditary, With Amyloidosis
Familial Cerebral Amyloid Angiopathy
HCHWA
Hereditary Cerebral Amyloid Angiopathy
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
Hereditary Cerebral Hemorrhage With Amyloidosis
Icelandic Type Amyloidosis
Icelandic Type Hereditary Cerebral Amyloid Angiopathy

Persistent link   https://www.medvik.cz/link/D028243
Definition

A familial disorder marked by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES.

DUI
D028243 MeSH Browser
CUI
M0334468
Previous indexing
Amyloidosis (1974-1991); Cerebrovascular Disorders (1974-1991); Cerebral Amyloid Angiopathy (1992-2001)
History note
2002; for CEREBRAL AMYLOID ANGIOPATHY, FAMILIAL use CEREBRAL AMYLOID ANGIOPATHY 2000-2001
Public note
2002; for CEREBRAL AMYLOID ANGIOPATHY, FAMILIAL see CEREBRAL AMYLOID ANGIOPATHY 2000-2001

Allowable subheadings

BL
blood 0
CF
cerebrospinal fluid 0
CI
chemically induced 0
CL
classification 0
CO
complications 0
DI
diagnosis 0
DG
diagnostic imaging 0
DH
diet therapy 0
DT
drug therapy 0
EC
economics 0
EM
embryology 0
EN
enzymology 0
EP
epidemiology 0
EH
ethnology 0
ET
etiology 0
GE
genetics 0
HI
history 0
IM
immunology 0
ME
metabolism 0
MI
microbiology 0
MO
mortality 0
NU
nursing 0
PS
parasitology 0
PA
pathology 0
PP
physiopathology 1
PC
prevention & control 0
PX
psychology 0
RT
radiotherapy 0
RH
rehabilitation 0
SU
surgery 0
TH
therapy 0
UR
urine 0
VE
veterinary 0
VI
virology 0

C Diseases
C10 Nervous System Diseases 1 877
C10.228 Central Nervous System Diseases 806
C10.228.140 Brain Diseases 1 177
C10.228.140.163 Brain Diseases, Metabolic 84
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn 26
C10.228.140.163.100.084 Adrenoleukodystrophy 41
C10.228.140.163.100.168 Cerebral Amyloid Angiopathy, Familial 1
C10.228.140.163.100.320 Galactosemias 44
C10.228.140.163.100.355 Hartnup Disease 2
C10.228.140.163.100.360 Hepatolenticular Degeneration 243
C10.228.140.163.100.362 Hereditary Central Nervous System Demyelinating Diseases 11
C10.228.140.163.100.365 Homocystinuria 107
C10.228.140.163.100.375 Hyperglycinemia, Nonketotic 7
C10.228.140.163.100.380 Hyperlysinemias
C10.228.140.163.100.412 Leigh Disease 26
C10.228.140.163.100.425 Lesch-Nyhan Syndrome 20
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System 13
C10.228.140.163.100.520 Maple Syrup Urine Disease 8
C10.228.140.163.100.535 MELAS Syndrome 17
C10.228.140.163.100.540 Menkes Kinky Hair Syndrome 12
C10.228.140.163.100.545 MERRF Syndrome 4
C10.228.140.163.100.593 Mevalonate Kinase Deficiency 16
C10.228.140.163.100.640 Oculocerebrorenal Syndrome 9
C10.228.140.163.100.687 Phenylketonurias 285
C10.228.140.163.100.725 Pyruvate Carboxylase Deficiency Disease
C10.228.140.163.100.750 Pyruvate Dehydrogenase Complex Deficiency Disease 9
C10.228.140.163.100.813 Refsum Disease 6
C10.228.140.163.100.844 Refsum Disease, Infantile
C10.228.140.163.100.875 Tyrosinemias 18
C10.228.140.163.100.937 Urea Cycle Disorders, Inborn 7
C10.228.140.163.100.968 Zellweger Syndrome 10
C10.228.140.300 Cerebrovascular Disorders 1 646
C10.228.140.300.275 Cerebral Small Vessel Diseases 7
C10.228.140.300.275.249 CADASIL 8
C10.228.140.300.275.311 Cerebral Amyloid Angiopathy, Familial 1
C10.228.140.300.275.374 Fabry Disease 187
C10.228.140.300.275.500 MELAS Syndrome 17
C10.228.140.300.275.600 Microscopic Polyangiitis 30
C10.228.140.300.275.800 Stroke, Lacunar 8
C10.228.140.300.510 Intracranial Arterial Diseases 43
C10.228.140.300.510.200 Cerebral Arterial Diseases 33
C10.228.140.300.510.200.200 Cerebral Amyloid Angiopathy 24
C10.228.140.300.510.200.200.160 Cerebral Amyloid Angiopathy, Familial 1
C14 Cardiovascular Diseases 10 491
C14.907 Vascular Diseases 1 789
C14.907.253 Cerebrovascular Disorders 1 646
C14.907.253.329 Cerebral Small Vessel Diseases 7
C14.907.253.329.249 CADASIL 8
C14.907.253.329.311 Cerebral Amyloid Angiopathy, Familial 1
C14.907.253.329.374 Fabry Disease 187
C14.907.253.329.500 MELAS Syndrome 17
C14.907.253.329.600 Microscopic Polyangiitis 30
C14.907.253.329.800 Stroke, Lacunar 8
C14.907.253.560 Intracranial Arterial Diseases 43
C14.907.253.560.200 Cerebral Arterial Diseases 33
C14.907.253.560.200.200 Cerebral Amyloid Angiopathy 24
C14.907.253.560.200.200.160 Cerebral Amyloid Angiopathy, Familial 1
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.565 Metabolism, Inborn Errors 711
C16.320.565.176 Amyloidosis, Familial 16
C16.320.565.176.050 Amyloid Neuropathies, Familial 20
C16.320.565.176.160 Cerebral Amyloid Angiopathy, Familial 1
C16.320.565.189 Brain Diseases, Metabolic, Inborn 26
C16.320.565.189.084 Adrenoleukodystrophy 41
C16.320.565.189.168 Cerebral Amyloid Angiopathy, Familial 1
C16.320.565.189.320 Galactosemias 44
C16.320.565.189.355 Hartnup Disease 2
C16.320.565.189.360 Hepatolenticular Degeneration 243
C16.320.565.189.362 Hereditary Central Nervous System Demyelinating Diseases 11
C16.320.565.189.365 Homocystinuria 107
C16.320.565.189.375 Hyperglycinemia, Nonketotic 7
C16.320.565.189.380 Hyperlysinemias
C16.320.565.189.412 Leigh Disease 26
C16.320.565.189.425 Lesch-Nyhan Syndrome 20
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System 13
C16.320.565.189.520 Maple Syrup Urine Disease 8
C16.320.565.189.535 MELAS Syndrome 17
C16.320.565.189.540 Menkes Kinky Hair Syndrome 12
C16.320.565.189.545 MERRF Syndrome 4
C16.320.565.189.593 Mevalonate Kinase Deficiency 16
C16.320.565.189.640 Oculocerebrorenal Syndrome 9
C16.320.565.189.687 Phenylketonurias 285
C16.320.565.189.725 Pyruvate Carboxylase Deficiency Disease
C16.320.565.189.750 Pyruvate Dehydrogenase Complex Deficiency Disease 9
C16.320.565.189.813 Refsum Disease 6
C16.320.565.189.844 Refsum Disease, Infantile
C16.320.565.189.875 Tyrosinemias 18
C16.320.565.189.937 Urea Cycle Disorders, Inborn 7
C16.320.565.189.968 Zellweger Syndrome 10
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 196
C18.452.132 Brain Diseases, Metabolic 84
C18.452.132.100 Brain Diseases, Metabolic, Inborn 26
C18.452.132.100.084 Adrenoleukodystrophy 41
C18.452.132.100.168 Cerebral Amyloid Angiopathy, Familial 1
C18.452.132.100.320 Galactosemias 44
C18.452.132.100.355 Hartnup Disease 2
C18.452.132.100.360 Hepatolenticular Degeneration 243
C18.452.132.100.362 Hereditary Central Nervous System Demyelinating Diseases 11
C18.452.132.100.365 Homocystinuria 107
C18.452.132.100.375 Hyperglycinemia, Nonketotic 7
C18.452.132.100.380 Hyperlysinemias
C18.452.132.100.412 Leigh Disease 26
C18.452.132.100.425 Lesch-Nyhan Syndrome 20
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System 13
C18.452.132.100.520 Maple Syrup Urine Disease 8
C18.452.132.100.535 MELAS Syndrome 17
C18.452.132.100.540 Menkes Kinky Hair Syndrome 12
C18.452.132.100.545 MERRF Syndrome 4
C18.452.132.100.593 Mevalonate Kinase Deficiency 16
C18.452.132.100.640 Oculocerebrorenal Syndrome 9
C18.452.132.100.687 Phenylketonurias 285
C18.452.132.100.725 Pyruvate Carboxylase Deficiency Disease
C18.452.132.100.750 Pyruvate Dehydrogenase Complex Deficiency Disease 9
C18.452.132.100.813 Refsum Disease 6
C18.452.132.100.844 Refsum Disease, Infantile
C18.452.132.100.875 Tyrosinemias 18
C18.452.132.100.937 Urea Cycle Disorders, Inborn 7
C18.452.132.100.968 Zellweger Syndrome 10
C18.452.648 Metabolism, Inborn Errors 711
C18.452.648.176 Amyloidosis, Familial 16
C18.452.648.176.050 Amyloid Neuropathies, Familial 20
C18.452.648.176.160 Cerebral Amyloid Angiopathy, Familial 1
C18.452.648.189 Brain Diseases, Metabolic, Inborn 26
C18.452.648.189.084 Adrenoleukodystrophy 41
C18.452.648.189.168 Cerebral Amyloid Angiopathy, Familial 1
C18.452.648.189.320 Galactosemias 44
C18.452.648.189.355 Hartnup Disease 2
C18.452.648.189.360 Hepatolenticular Degeneration 243
C18.452.648.189.362 Hereditary Central Nervous System Demyelinating Diseases 11
C18.452.648.189.365 Homocystinuria 107
C18.452.648.189.375 Hyperglycinemia, Nonketotic 7
C18.452.648.189.380 Hyperlysinemias
C18.452.648.189.412 Leigh Disease 26
C18.452.648.189.425 Lesch-Nyhan Syndrome 20
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System 13
C18.452.648.189.520 Maple Syrup Urine Disease 8
C18.452.648.189.535 MELAS Syndrome 17
C18.452.648.189.540 Menkes Kinky Hair Syndrome 12
C18.452.648.189.545 MERRF Syndrome 4
C18.452.648.189.593 Mevalonate Kinase Deficiency 16
C18.452.648.189.640 Oculocerebrorenal Syndrome 9
C18.452.648.189.687 Phenylketonurias 285
C18.452.648.189.725 Pyruvate Carboxylase Deficiency Disease
C18.452.648.189.750 Pyruvate Dehydrogenase Complex Deficiency Disease 9
C18.452.648.189.813 Refsum Disease 6
C18.452.648.189.844 Refsum Disease, Infantile
C18.452.648.189.875 Tyrosinemias 18
C18.452.648.189.937 Urea Cycle Disorders, Inborn 7
C18.452.648.189.968 Zellweger Syndrome 10
C18.452.845 Proteostasis Deficiencies 6
C18.452.845.500 Amyloidosis 471
C18.452.845.500.075 Amyloidosis, Familial 16
C18.452.845.500.075.050 Amyloid Neuropathies, Familial 20
C18.452.845.500.075.160 Cerebral Amyloid Angiopathy, Familial 1
C18.452.845.500.100 Cerebral Amyloid Angiopathy 24
C18.452.845.500.100.160 Cerebral Amyloid Angiopathy, Familial 1

Add