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Amyloidosis, Familial
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Amyloidosis, Familial
Tree Number(s)
C16.320.565.176
C18.452.648.176
C18.452.845.500.075
Unique ID
D028226
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D028226
Scope Note
Diseases in which there is a familial pattern of
AMYLOIDOSIS
.
Entry Term(s)
Amyloidosis, Hereditary
Previous Indexing
Amyloidosis (1966-2001)
Public MeSH Note
2002
History Note
2002
Date Established
2002/01/01
Date of Entry
2001/07/25
Revision Date
2017/06/20
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
Amino Acid Transport Disorders, Inborn [C16.320.565.151]
Amyloidosis, Familial [C16.320.565.176]
Amyloid Neuropathies, Familial [C16.320.565.176.050]
Cerebral Amyloid Angiopathy, Familial [C16.320.565.176.160]
Brain Diseases, Metabolic, Inborn [C16.320.565.189]
Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
Cytochrome-c Oxidase Deficiency [C16.320.565.240]
Hyperbilirubinemia, Hereditary [C16.320.565.300]
Lipid Metabolism, Inborn Errors [C16.320.565.398]
Lysosomal Storage Diseases [C16.320.565.595]
Metal Metabolism, Inborn Errors [C16.320.565.618]
Peroxisomal Disorders [C16.320.565.663]
Progeria [C16.320.565.753]
Purine-Pyrimidine Metabolism, Inborn Errors [C16.320.565.798]
Renal Tubular Transport, Inborn Errors [C16.320.565.893]
Steroid Metabolism, Inborn Errors [C16.320.565.925]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
Amino Acid Transport Disorders, Inborn [C18.452.648.151]
Amyloidosis, Familial [C18.452.648.176]
Amyloid Neuropathies, Familial [C18.452.648.176.050]
Cerebral Amyloid Angiopathy, Familial [C18.452.648.176.160]
Brain Diseases, Metabolic, Inborn [C18.452.648.189]
Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
Hyperbilirubinemia, Hereditary [C18.452.648.300]
Lipid Metabolism, Inborn Errors [C18.452.648.398]
Lysosomal Storage Diseases [C18.452.648.595]
Metal Metabolism, Inborn Errors [C18.452.648.618]
Peroxisomal Disorders [C18.452.648.663]
Progeria [C18.452.648.753]
Purine-Pyrimidine Metabolism, Inborn Errors [C18.452.648.798]
Renal Tubular Transport, Inborn Errors [C18.452.648.893]
Steroid Metabolism, Inborn Errors [C18.452.648.925]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Proteostasis Deficiencies [C18.452.845]
Amyloidosis [C18.452.845.500]
Amyloid Neuropathies [C18.452.845.500.050]
Amyloidosis, Familial [C18.452.845.500.075]
Amyloid Neuropathies, Familial [C18.452.845.500.075.050]
Cerebral Amyloid Angiopathy, Familial [C18.452.845.500.075.160]
Cerebral Amyloid Angiopathy [C18.452.845.500.100]
Immunoglobulin Light-chain Amyloidosis [C18.452.845.500.550]
Expand All
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Amyloidosis, Familial
Preferred
Concept UI
M0383396
Scope Note
Diseases in which there is a familial pattern of
AMYLOIDOSIS
.
Terms
Amyloidosis, Familial
Preferred Term
Term UI
T442090
Date
04/06/2001
LexicalTag
NON
ThesaurusID
NLM (2002)
Amyloidosis, Hereditary
Term UI
T440254
Date
03/21/2001
LexicalTag
NON
ThesaurusID
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