Traduction de «episcleritis nos » (Anglais → Français) :

episcleritis fugax | episcleritis periodica fugax | partial episcleritis fugax
épisclérite périodique fugace

furunculoid episcleritis | furunculoid metastatic episcleritis
épisclérite furonculiforme de Kramer | épisclérite métastatique furonculiforme de Kramer

episcleral arteries
artères épisclerales

Episcleritis, NOS
épisclérite

Syphilitic episcleritis (A52.7+) Tuberculous episcleritis (A18.5+) Zoster scleritis (B02.3+)
Episclérite:syphilitique (A52.7+) | tuberculeuse (A18.5+) | Sclérite zostérienne (B02.3+)

episcleritis
épisclérite [ épiscléritis ]

Glomerular disease in syphilis+ (N08.0*) Gumma (syphilitic) | Late or tertiary syphilis | any sites, except those classified to A52.0-A52.3 | Late syphilitic:bursitis+ (M73.1*) | chorioretinitis+ (H32.0*) | episcleritis+ (H19.0*) | female pelvic inflammatory disease+ (N74.2*) | leukoderma+ (L99.8*) | oculopathy NEC+ (H58.8*) | peritonitis+ (K67.2*) | Syphilis [stage unspecified] of:bone+ (M90.2*) | liver+ (K77.0*) | lung+ (J99.8*) | muscle+ (M63.0*) | synovium+ (M68.0*)
Affection inflammatoire des organes pelviens de la femme+ (N74.2*) | Bursite+ (M73.1*) | Choriorétinite+ (H32.0*) | Episclérite+ (H19.0*) | Leucodermie+ (L99.8*) | Oculopathie NCA+ (H58.8*) | Péritonite+ (K67.2*) | syphilitique tardive | Glomérulite syphilitique+ (N08.0*) Gomme (syphilitique) | Syphilis tardive ou tertiaire | toute localisation, sauf celles classées en A52.0-A52.3 | Synovite syphilitique [stade non précisé]+ (M68.0*) Syphilis [stade non précisé]:hépatique+ (K77.0*) | musculaire+ (M63.0*) | osseuse+ (M90.2*) | pulmonaire+ (J99.8*)

Tuberculous:chorioretinitis+ (H32.0*) | episcleritis+ (H19.0*) | interstitial keratitis+ (H19.2*) | iridocyclitis+ (H22.0*) | keratoconjunctivitis (interstitial)(phlyctenular)+ (H19.2*)
Choriorétinite+ (H32.0*) | Episclérite+ (H19.0*) | Iridocyclite+ (H22.0*) | Kératite interstitielle+ (H19.2*) | Kératoconjonctivite (interstitielle) (phlycténulaire)+ (H19.2*) | tuberculeuse

A rare and isolated orofacial defect with manifestation of incomplete median clefts of both the lower lip (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper g
fente labiale médiane supérieure et inférieure, forme familiale

An X-linked disorder of purine metabolism comprised of two forms: an early-onset severe form with characteristics of gout, urolithiasis, and neurodevelopmental anomalies (severe PRPP synthetase superactivity) and a mild late-onset form with no neurol
hyperactivité de la phosphoribosylpyrophosphate synthétase