Amyloidosis, Familial [familiární amyloidóza]

topical
16
Terms

amyloidóza familiární

 

Amyloidosis, Hereditary

Persistent link   https://www.medvik.cz/link/D028226
Definition

Diseases in which there is a familial pattern of AMYLOIDOSIS.

DUI
D028226 MeSH Browser
CUI
M0383396
Previous indexing
Amyloidosis (1966-2001)
History note
2002
Public note
2002

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 6
DI
diagnosis 9
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 5
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 4
GE
genetics 7
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 1
PP
physiopathology 2
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 4
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.565 Metabolism, Inborn Errors 714
C16.320.565.100 Amino Acid Metabolism, Inborn Errors 124
C16.320.565.151 Amino Acid Transport Disorders, Inborn 1
C16.320.565.176 Amyloidosis, Familial 16
C16.320.565.176.050 Amyloid Neuropathies, Familial 21
C16.320.565.176.160 Cerebral Amyloid Angiopathy, Familial 1
C16.320.565.189 Brain Diseases, Metabolic, Inborn 28
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors 36
C16.320.565.240 Cytochrome-c Oxidase Deficiency 27
C16.320.565.300 Hyperbilirubinemia, Hereditary 35
C16.320.565.398 Lipid Metabolism, Inborn Errors 154
C16.320.565.595 Lysosomal Storage Diseases 73
C16.320.565.618 Metal Metabolism, Inborn Errors 16
C16.320.565.663 Peroxisomal Disorders 20
C16.320.565.753 Progeria 27
C16.320.565.798 Purine-Pyrimidine Metabolism, Inborn Errors 41
C16.320.565.893 Renal Tubular Transport, Inborn Errors 36
C16.320.565.925 Steroid Metabolism, Inborn Errors 7
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 200
C18.452.648 Metabolism, Inborn Errors 714
C18.452.648.100 Amino Acid Metabolism, Inborn Errors 124
C18.452.648.151 Amino Acid Transport Disorders, Inborn 1
C18.452.648.176 Amyloidosis, Familial 16
C18.452.648.176.050 Amyloid Neuropathies, Familial 21
C18.452.648.176.160 Cerebral Amyloid Angiopathy, Familial 1
C18.452.648.189 Brain Diseases, Metabolic, Inborn 28
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors 36
C18.452.648.300 Hyperbilirubinemia, Hereditary 35
C18.452.648.398 Lipid Metabolism, Inborn Errors 154
C18.452.648.595 Lysosomal Storage Diseases 73
C18.452.648.618 Metal Metabolism, Inborn Errors 16
C18.452.648.663 Peroxisomal Disorders 20
C18.452.648.753 Progeria 27
C18.452.648.798 Purine-Pyrimidine Metabolism, Inborn Errors 41
C18.452.648.893 Renal Tubular Transport, Inborn Errors 36
C18.452.648.925 Steroid Metabolism, Inborn Errors 7
C18.452.845 Proteostasis Deficiencies 6
C18.452.845.500 Amyloidosis 475
C18.452.845.500.050 Amyloid Neuropathies 17
C18.452.845.500.075 Amyloidosis, Familial 16
C18.452.845.500.075.050 Amyloid Neuropathies, Familial 21
C18.452.845.500.075.160 Cerebral Amyloid Angiopathy, Familial 1
C18.452.845.500.100 Cerebral Amyloid Angiopathy 24
C18.452.845.500.550 Immunoglobulin Light-chain Amyloidosis 37

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