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Translation of "syndrome de cataracte-freins " (French → English) :
TERMINOLOGY
see also In-Context Translations below syndrome de cataracte-freins buccaux anormaux-retard de croissance
Wellesley Carman French syndrome
SNOMEDCT-BE (disorder) / 715988005
SNOMEDCT-BE (disorder) / 715988005
syndrome de cataracte congénitale-cardiomyopathie hypertrophique-myopathie mitochondriale
A mitochondrial disease with characteristics of cataracts, hypertrophic cardiomyopathy, muscle weakness and lactic acidosis after exercise. May present in two forms, a neonatal lethal form or a chronic form. Hypertrophic cardiomyopathy is diagnosed a
SNOMEDCT-BE (disorder) / 717812000
SNOMEDCT-BE (disorder) / 717812000
syndrome de cataracte congénitale-surdité-retard de développement sévère
A rare genetic lethal neurometabolic disease characterized by congenital cataracts, sensorineural hearing loss, severe psychomotor developmental delay, severe generalized muscular hypotonia and central nervous system abnormalities (including cerebell
SNOMEDCT-BE (disorder) / 773648002
SNOMEDCT-BE (including cerebell / 773648002
syndrome de cataracte juvénile-microcornée-glucosurie rénale
Juvenile cataract, microcornea, renal glucosuria syndrome
SNOMEDCT-BE (disorder) / 722457005
SNOMEDCT-BE (disorder) / 722457005
Modificateurs Les subdivisions suivantes peuvent être utilisées comme quatrième chiffre avec les rubriques E10-E14: Code Titre .0 Avec coma Coma:diabétique, avec ou sans acidocétose:hyperglycémique | hyperosmolaire | hyperglycémique SAI | .1 Avec acidocétose Acidocétose | Acidose | diabétique, sans mention de coma | .2+ Avec complications rénales Glomérulonéphrite intracapillaire (N08.3*) Néphropathie
diabétique (N08.3*) Syndrome de Kimmelstiel-Wilson (N08.3*) .3+ Avec comp
lications oculaires Cataracte (H28.0*) | Rétinopathie (H36.0*)
...[+++] | diabétique | .4+ Avec complications neurologiques Amyotrophie (G73.0*) | Mononévrite (G59.0*) | Neuropathie végétative (G99.0*) | Polynévrite (G63.2*) système nerveux autonome (G99.0*) | diabétique | .5 Avec complications vasculaires périphériques Angiopathie périphérique+ (I79.2*) | Gangrène | Ulcère | diabétique | .6 Avec autres complications précisées Arthropathie diabétique (M14.2*) nerveuse+ (M14.6*) | .7 Avec complications multiples .8 Avec complications non précisées .9 Sans complication | Coma:diabétique, avec ou sans acidocétose:hyperglycémique | hyperosmolaire | hyperglycémique SAI | Acidocétose | Acidose | diabétique, sans mention de coma | Glomérulonéphrite intracapillaire (N08.3*) Néphropathie diabétique (N08.3*) Syndrome de Kimmelstiel-Wilson (N08.3*) | Cataracte (H28.0*) | Rétinopathie (H36.0*) | diabétique | Amyotrophie (G73.0*) | Mononévrite (G59.0*) | Neuropathie végétative (G99.0*) | Polynévrite (G63.2*) système nerveux autonome (G99.0*) | diabétique | Angiopathie périphérique+ (I79.2*) | Gangrène | Ulcère | diabétique | Arthropathie diabétique (M14.2*) nerveuse+ (M14.6*)
Modifiers The following fourth-character subdivisions are for use with categories E10-E14: Code Title .0 With coma Diabetic:coma with or without ketoacidosis | hyperosmolar coma | hypoglycaemic coma | Hyperglycaemic coma NOS .1 With ketoacidosis Diabetic:acidosis | ketoacidosis | without mention of coma | .2+ With renal complications Diabetic nephropathy (N08.3*) Intracapillary glomerulonephrosis (N08.3*)
Kimmelstiel-Wilson syndrome (N08.3*) .3+ With ophthalmic complications Diabetic:cataract (H28.0*) | retinopathy (H36.0*) | .4+ With neurological complications Diabetic:amyotrophy (G73.0*) | autonomic neuropathy (G99.0*) | mononeuropathy
...[+++] (G59.0*) | polyneuropathy (G63.2*) autonomic (G99.0*) | .5 With peripheral circulatory complications Diabetic:gangrene | peripheral angiopathy+ (I79.2*) | ulcer | .6 With other specified complications Diabetic arthropathy+ (M14.2*) Neuropathic diabetic arthropathy+ (M14.6*) .7 With multiple complications .8 With unspecified complications .9 Without complications | Diabetic:coma with or without ketoacidosis | hyperosmolar coma | hypoglycaemic coma | Hyperglycaemic coma NOS | Diabetic:acidosis | ketoacidosis | without mention of coma | Diabetic nephropathy (N08.3*) Intracapillary glomerulonephrosis (N08.3*) Kimmelstiel-Wilson syndrome (N08.3*) | Diabetic:cataract (H28.0*) | retinopathy (H36.0*) | Diabetic:amyotrophy (G73.0*) | autonomic neuropathy (G99.0*) | mononeuropathy (G59.0*) | polyneuropathy (G63.2*) autonomic (G99.0*) | Diabetic:gangrene | peripheral angiopathy+ (I79.2*) | ulcer | Diabetic arthropathy+ (M14.2*) Neuropathic diabetic arthropathy+ (M14.6*)WORLD HEALTH ORGANIZATION ICD-10: E10-E14
WORLD HEALTH ORGANIZATION ICD-10: E10-E14
syndrome d'atrophie optique-cataracte autosomique dominante
Autosomal dominant optic atrophy type 3
SNOMEDCT-BE (disorder) / 719517009
SNOMEDCT-BE (disorder) / 719517009
syndrome de porencéphalie-microcéphalie-cataracte bilatérale congénitale
A rare genetic central nervous system malformation syndrome characterized by bilateral congenital cataracts and severe hemorrhagic destruction of the brain parenchyma with associated massive cystic degeneration, enlarged ventricles and subependymal c
SNOMEDCT-BE (disorder) / 773627004
SNOMEDCT-BE (disorder) / 773627004
syndrome d'amyotrophie spinale-malformation de Dandy-Walker-cataracte
Syndrome with characteristics of infantile symmetrical distal muscle weakness and atrophy of the lower limbs, bilateral anterior polar cataracts and Dandy-Walker malformation. It has been described in two brothers. No sensorineural or cognitive defic
SNOMEDCT-BE (disorder) / 723612001
SNOMEDCT-BE (disorder) / 723612001
syndrome d'hypogonadisme hypergonadotrope-cataracte
Lubinsky syndrome
SNOMEDCT-BE (disorder) / 721233005
SNOMEDCT-BE (disorder) / 721233005
syndrome d'hypoplasie fovéale-cataracte présénile
A rare genetic ocular disease with characteristics of congenital nystagmus (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus an
SNOMEDCT-BE (disorder) / 778042000
SNOMEDCT-BE (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus an / 778042000
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syndrome de cataracte-freins
Date index:2023-03-06 -
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