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1 hereditary amyloidosis
Медицина: наследственный амилоидоз (генетический)Универсальный англо-русский словарь > hereditary amyloidosis
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2 hereditary amyloidosis
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3 hereditary cerebral hemorrhage with amyloidosis of the Dutch type
Универсальный англо-русский словарь > hereditary cerebral hemorrhage with amyloidosis of the Dutch type
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4 наследственный амилоидоз
Medicine: hereditary amyloidosis (генетический)Универсальный русско-английский словарь > наследственный амилоидоз
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5 генетический амилоидоз
genetic [hereditary] amyloidosisБольшой русско-английский медицинский словарь > генетический амилоидоз
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6 الداء النشواني الوراثي المعل للأعصاب
hereditary neuropathic amyloidosisArabic-English Medical Dictionary > الداء النشواني الوراثي المعل للأعصاب
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7 наследственный амилоидоз
hereditary [genetic] amyloidosisБольшой русско-английский медицинский словарь > наследственный амилоидоз
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8 N07
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9 N07.0
рус Незначительные гломерулярные нарушенияeng Hereditary nephropathy, not elsewhere classified. (Excludes: ) Alport's syndrome ( Q87.8), hereditary amyloid nephropathy ( E85.0), nail patella syndrome ( Q87.2), non-neuropathic heredofamilial amyloidosis ( E85.0). Minor glomerular abnormality. Minimal change lesion -
10 N07.1
рус Очаговые и сегментарные гломерулярные поврежденияeng Hereditary nephropathy, not elsewhere classified. (Excludes: ) Alport's syndrome ( Q87.8), hereditary amyloid nephropathy ( E85.0), nail patella syndrome ( Q87.2), non-neuropathic heredofamilial amyloidosis ( E85.0). Focal and segmental glomerular lesions. Focal and segmental: hyalinosis, sclerosis. Focal glomerulonephritis -
11 N07.2
рус Диффузный мембранозный гломерулонефритeng Hereditary nephropathy, not elsewhere classified. (Excludes: ) Alport's syndrome ( Q87.8), hereditary amyloid nephropathy ( E85.0), nail patella syndrome ( Q87.2), non-neuropathic heredofamilial amyloidosis ( E85.0). Diffuse membranous glomerulonephritis -
12 N07.3
рус Диффузный мезангиальный пролиферативный гломерулонефритeng Hereditary nephropathy, not elsewhere classified. (Excludes: ) Alport's syndrome ( Q87.8), hereditary amyloid nephropathy ( E85.0), nail patella syndrome ( Q87.2), non-neuropathic heredofamilial amyloidosis ( E85.0). Diffuse mesangial proliferative glomerulonephritis -
13 N07.4
рус Диффузный эндокапиллярный пролиферативный гломерулонефритeng Hereditary nephropathy, not elsewhere classified. (Excludes: ) Alport's syndrome ( Q87.8), hereditary amyloid nephropathy ( E85.0), nail patella syndrome ( Q87.2), non-neuropathic heredofamilial amyloidosis ( E85.0). Diffuse endocapillary proliferative glomerulonephritis -
14 N07.5
рус Диффузный мезангиокапиллярный гломерулонефритeng Hereditary nephropathy, not elsewhere classified. (Excludes: ) Alport's syndrome ( Q87.8), hereditary amyloid nephropathy ( E85.0), nail patella syndrome ( Q87.2), non-neuropathic heredofamilial amyloidosis ( E85.0). Diffuse mesangiocapillary glomerulonephritis. Membranoproliferative glomerulonephritis, types 1 and 3, or NOS -
15 N07.6
рус Болезнь плотного осадкаeng Hereditary nephropathy, not elsewhere classified. (Excludes: ) Alport's syndrome ( Q87.8), hereditary amyloid nephropathy ( E85.0), nail patella syndrome ( Q87.2), non-neuropathic heredofamilial amyloidosis ( E85.0). Dense deposit disease. Membranoproliferative glomerulonephritis, type 2 -
16 N07.7
рус Диффузный серповидный гломерулонефритeng Hereditary nephropathy, not elsewhere classified. (Excludes: ) Alport's syndrome ( Q87.8), hereditary amyloid nephropathy ( E85.0), nail patella syndrome ( Q87.2), non-neuropathic heredofamilial amyloidosis ( E85.0). Diffuse crescentic glomerulonephritis. Extracapillary glomerulonephritis -
17 N07.8
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18 N07.9
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19 наследственная церебральная геморрагия с амилоидозом голландского типа
Универсальный русско-английский словарь > наследственная церебральная геморрагия с амилоидозом голландского типа
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20 E85.0
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- 2
См. также в других словарях:
Hereditary amyloidosis — A familial (inherited) disorder in which protein deposits (amyloid) accumulate in one or more organ systems in the body. Hereditary amyloidosis is a relatively uncommon cause of amyloidosis. The more common forms of amyloidosis are primary an… … Medical dictionary
Transthyretin-related hereditary amyloidosis — Classification and external resources OMIM 105210 eMedicine article/335301 Familial amyloid polyneuropathy (FAP), also c … Wikipedia
Amyloidosis, hereditary — A familial (inherited) disorder in which protein deposits (amyloid) accumulate in one or more organ systems in the body. Hereditary amyloidosis is a relatively uncommon cause of amyloidosis. The more common forms of amyloidosis are primary an… … Medical dictionary
amyloidosis — /am euh loy doh sis/, n., pl. amyloidoses / seez/. Pathol. 1. a deposit of amyloid in tissues or organs. 2. the diseased state resulting from this deposit. [1895 1900; AMYLOID + OSIS] * * * ▪ pathology disease characterized by the… … Universalium
Amyloidosis — A disorder that results from the abnormal deposition of a particular protein, called amyloid, in various tissues of the body. Amyloid protein can be deposited in a localized area, and not be harmful, or in can cause serious changes in virtually… … Medical dictionary
Organ-limited amyloidosis — Classification and external resources ICD 10 E85.4 ICD 9 277.3 Organ limited amyloidosis … Wikipedia
Haemodialysis-associated amyloidosis — Classification and external resources ICD 10 E85.3 ICD 9 277.3 … Wikipedia
ATTR amyloidosis — the most common form of hereditary amyloidosis, in which any of numerous mutations of the TTR gene (locus: 18q11.2 q12.1), which encodes transthyretin, cause systemic autosomal dominant disorders characterized by polyneuropathies,… … Medical dictionary
familial amyloidosis — hereditary a … Medical dictionary
heredofamilial amyloidosis — hereditary a … Medical dictionary
Familial renal amyloidosis — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 33335 ICD10 = ICD10|E|85|0|e|70 ICD9 = ICD9|277.3 ICDO = OMIM = 105200 MedlinePlus = eMedicineSubj = med eMedicineTopic = 3379 MeshID = Familial renal amyloidosis (or familial visceral… … Wikipedia
