Amyloid Neuropathies, Familial [familiární amyloidové neuropatie]
- Terms
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amyloidová neuropatie, typ I
amyloidová polyneuropatie, britská forma
amyloidová polyneuropatie, britský typ
amyloidová polyneuropatie, Iowa forma
amyloidová polyneuropatie, Iowa typ
amyloidová polyneuropatie, švýcarská forma
amyloidová polyneuropatie, švýcarský typ
familiární amyloidová neuropatie, portugalská forma
familiární amyloidová neuropatie, portugalský typ
familiární amyloidová polyneuropatie, apalačská forma
familiární amyloidová polyneuropatie, apalačský typ
familiární amyloidová polyneuropatie, forma IV
familiární amyloidová polyneuropatie, forma V
familiární amyloidová polyneuropatie, forma VI
familiární amyloidová polyneuropatie, typ III
familiární amyloidová polyneuropatie, typ IV
familiární amyloidová polyneuropatie, typ V
familiární amyloidová polyneuropatie, typ VI
familiární amyloidová polyneuropatie, židovská forma
familiární amyloidová polyneuropatie, židovský typ
familiární polyneuropatie při amyloidóze
neuropatie při amyloidóze familiární
portugalská polyneuritická amyloidóza
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Amyloid Neuropathy Type 1
Amyloid Polyneuropathy, British Type
Amyloid Polyneuropathy, Iowa Type
Amyloid Polyneuropathy, Swiss Type
Appalachian Type Familial Amyloid Polyneuropathy
British Type Amyloid Polyneuropathy
Cerebral Amyloid Angiopathy, British Type
Familial Amyloid Neuropathy, Andrade Type
Familial Amyloid Neuropathy, Finnish Type
Familial Amyloid Neuropathy, Portuguese Type
Familial Amyloid Polyneuropathies
Familial Amyloid Polyneuropathy, Appalachian Type
Familial Amyloid Polyneuropathy, Jewish Type
Familial Amyloid Polyneuropathy, Type I
Familial Amyloid Polyneuropathy, Type II
Familial Amyloid Polyneuropathy, Type III
Familial Amyloid Polyneuropathy, Type IV
Familial Amyloid Polyneuropathy, Type V
Familial Amyloid Polyneuropathy, Type VI
Familial Portuguese Polyneuritic Amyloidosis
Finnish Type Familial Amyloid Neuropathy
Hereditary Neuropathic Amyloidosis
Iowa Type Amyloid Polyneuropathy
Jewish Type Familial Amyloid Polyneuropathy
Neuropathic Amyloid Syndrome
Polyneuritic Amyloidosis, Portuguese
Portuguese Polyneuritic Amyloidosis
Portuguese Type Familial Amyloid Neuropathy
Swiss Type Amyloid Polyneuropathy
Type I Familial Amyloid Polyneuropathy
Type II Familial Amyloid Polyneuropathy
Type III Familial Amyloid Polyneuropathy
Type IV Familial Amyloid Polyneuropathy
Type V Familial Amyloid Polyneuropathy
Type VI Familial Amyloid Polyneuropathy
Wohlwill-Andrade Syndrome
Wohlwill-Corino Andrade Syndrome
Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.
- DUI
- D028227 MeSH Browser
- CUI
- M0026861
- Previous indexing
- Amyloidosis (1967-1993); Peripheral Nervous System Diseases (1967-1993); Amyloid Neuropathies (1994-2001)
- History note
- 2002; use AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES use AMYLOID NEUROPATHIES 1994-2001
- Public note
- 2002; see AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES see AMYLOID NEUROPATHIES 1994-2001
Allowable subheadings
- BL
- blood 0
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 0
- CL
- classification 1
- CO
- complications 1
- DI
- diagnosis 16
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 8
- EC
- economics 0
- EM
- embryology 0
- EN
- enzymology 0
- EP
- epidemiology 5
- EH
- ethnology 0
- ET
- etiology 1
- GE
- genetics 8
- HI
- history 0
- IM
- immunology 0
- ME
- metabolism 0
- MI
- microbiology 0
- MO
- mortality 0
- NU
- nursing 0
- PS
- parasitology 0
- PA
- pathology 6
- PP
- physiopathology 5
- PC
- prevention & control 1
- PX
- psychology 0
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 1
- TH
- therapy 8
- UR
- urine 0
- VE
- veterinary 1
- VI
- virology 0