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Translation of "Diffusion " (French → English) :
TERMINOLOGY
see also In-Context Translations below diffusion | diffusion
diffusion | spreading
UGENT - Medical terms -
UGENT - Medical terms -
Modificateurs Les subdivisions suivantes peuvent être utilisées comme quatrième chiffre avec les catégories N00-N07 pour classer les modifications morphologiques. Les subdivisions .0-.8 ne doivent être normalement utilisées que s'il y a eu identification précise (par biopsie rénale ou autopsie). Les catégories à trois caractères concernent les syndromes cliniques. Code Titre .0 Anomalies glomérulaires mineures Lésions minimes .1 Lésions glomérulaires segmentaires et focales Glomérulonéphrite focale Hyalinose | Sclérose | segmentaire et focale | .2 Glomérulon
éphrite membraneuse diffuse .3 Glomérulonéphrite proliférative mésangiale diffuse
...[+++] .4 Glomérulonéphrite proliférative endocapillaire diffuse .5 Glomérulonéphrite mésangiocapillaire diffuse Glomérulonéphrite membranoproliférative, types 1 et 3, ou SAI .6 Maladie à dépôt dense Glomérulonéphrite membranoproliférative, type 2 .7 Glomérulonéphrite diffuse en croissant Glomérulonéphrite extracapillaire .8 Autres Glomérulonéphrite proliférative SAI .9 Sans précision | Lésions minimes | Glomérulonéphrite focale Hyalinose | Sclérose | segmentaire et focale | Glomérulonéphrite membranoproliférative, types 1 et 3, ou SAI | Glomérulonéphrite membranoproliférative, type 2 | Glomérulonéphrite extracapillaire | Glomérulonéphrite proliférative SAI
Modifiers The following fourth-character subdivisions classify morphological changes and are for use with categories N00-N07. Subdivisions .0-.8 should not normally be used unless these have been specifically identified (e.g. by renal biopsy or autopsy). The three-character categories relate to clinical syndromes. Code Title .0 Minor glomerular abnormality Minimal change lesion .1 Focal and segmental glomerular lesions Focal and segmental:hyalinosis | sclerosis | Focal gl
omerulonephritis .2 Diffuse membranous glomerulonephritis .3 Diffuse mesangial proliferative glomerulonephritis .4 Diffuse endocapillary proliferative glomerulonephritis
...[+++] .5 Diffuse mesangiocapillary glomerulonephritis Membranoproliferative glomerulonephritis, types 1 and 3, or NOS .6 Dense deposit disease Membranoproliferative glomerulonephritis, type 2 .7 Diffuse crescentic glomerulonephritis Extracapillary glomerulonephritis .8 Other Proliferative glomerulonephritis NOS .9 Unspecified | Minimal change lesion | Focal and segmental:hyalinosis | sclerosis | Focal glomerulonephritis | Membranoproliferative glomerulonephritis, types 1 and 3, or NOS | Membranoproliferative glomerulonephritis, type 2 | Extracapillary glomerulonephritis | Proliferative glomerulonephritis NOSWORLD HEALTH ORGANIZATION ICD-10: N00-N08
WORLD HEALTH ORGANIZATION ICD-10: N00-N08
diffus | diffus
diffuse | widely distributed
UGENT - Medical terms -
UGENT - Medical terms -
fibrose pulmonaire interstitielle diffuse
Fibrosing alveolitis
SNOMEDCT-BE (disorder) / 196125002
SNOMEDCT-BE (disorder) / 196125002
syndrome de kératodermie palmoplantaire diffuse-acrocyanose
Syndrome with the association of diffuse palmoplantar keratoderma and acrocyanosis. It has been described in eight members of one family and in two sporadic cases. The mode of inheritance in the familial cases was autosomal dominant.
SNOMEDCT-BE (disorder) / 721096008
SNOMEDCT-BE (disorder) / 721096008
sclérose systémique, diffuse
Diffuse cutaneous scleroderma
SNOMEDCT-BE (disorder) / 128460000
SNOMEDCT-BE (disorder) / 128460000
goitre toxique diffus
Toxic diffuse goiter
SNOMEDCT-BE (disorder) / 267374005
SNOMEDCT-BE (disorder) / 267374005
spasmes diffus de l'œsophage
Barsony-Polgar syndrome
SNOMEDCT-BE (disorder) / 79962008
SNOMEDCT-BE (disorder) / 79962008
lymphome B diffus à grandes cellules positif au virus Epstein-Barr chez les personnes âgées
A rare form of diffuse large B-cell lymphoma occurring most commonly in patients over the age of 50 (usually between 70-75 years of age), without overt immunodeficiency, and presenting with nodal and extranodal involvement (in sites such as the stoma
SNOMEDCT-BE (disorder) / 716788007
SNOMEDCT-BE (usually between 70-75 years of age), without overt immunodeficiency, and presenting with nodal and extranodal involvement (in sites such as the stoma / 716788007
syndrome de rétinopathie ischémique-hyalinose digestive-calcifications cérébrales diffuses
Rambaud Gallian syndrome
SNOMEDCT-BE (disorder) / 724002003
SNOMEDCT-BE (disorder) / 724002003
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Diffusion
Date index:2021-12-17 -
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