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Eosinophilic granuloma
Eosinophilic granuloma of skin
Granuloma and granuloma-like lesions of oral mucosa
Granuloma faciale
Granuloma pyogenicum
Of oral mucosa
Verrucous xanthoma

Translation of "granuloma faciale " (English → French) :

Granuloma faciale [eosinophilic granuloma of skin]
https://icd.who.int/browse10/2 (...) (...) [HTML]
Granulome éosinophile de la peau
WORLD HEALTH ORGANIZATION ICD-10: L92.2
WORLD HEALTH ORGANIZATION ICD-10: L92.2
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Granuloma and granuloma-like lesions of oral mucosa
https://icd.who.int/browse10/2 (...) (...) [HTML]
Granulome et lésions pseudo-granulomateuses de la muqueuse buccale
WORLD HEALTH ORGANIZATION ICD-10: K13.4
WORLD HEALTH ORGANIZATION ICD-10: K13.4
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Eosinophilic granuloma | Granuloma pyogenicum | Verrucous xanthoma | of oral mucosa
https://icd.who.int/browse10/2 (...) (...) [HTML]
Granulome:éosinophile | pyogène | Xanthome verruqueux | de la muqueuse buccale
WORLD HEALTH ORGANIZATION ICD-10: K13.4
WORLD HEALTH ORGANIZATION ICD-10: K13.4
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Fibrous epulis Flabby ridge Giant cell epulis Peripheral giant cell granuloma Pyogenic granuloma of gingiva
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Crête gingivale flottante Epulis (à):cellules géantes | fibreux | Granulome:gingival pyogène | périphérique à cellules géantes
WORLD HEALTH ORGANIZATION ICD-10: K06.8
WORLD HEALTH ORGANIZATION ICD-10: K06.8
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Rare syndrome with characteristics of the combination of polyvalvular heart disease, short stature, facial anomalies and intellectual deficit. Dysplasia may involve the mitral, tricuspidal, aortic and pulmonary valves. Dysmorphic facial anomalies are
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syndrome de la maladie cardiaque polyvalvulaire
SNOMEDCT-BE (disorder) / 723448007
SNOMEDCT-BE (disorder) / 723448007
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https://browser.ihtsdotools.or (...) [HTML]
This syndrome is characterized by severe intellectual deficit, hypotonia, mild facial dysmorphism and aggressive behavior. It has been described in 10 male members spanning four generations of one family. The facial dysmorphism includes a high forehe
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syndrome de déficience intellectuelle liée à l'X-hypotonie-dysmorphie faciale-comportement agressif
SNOMEDCT-BE (disorder) / 719157002
SNOMEDCT-BE (disorder) / 719157002
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https://browser.ihtsdotools.or (...) [HTML]
This syndrome has features of fibuloulnar dysostosis with renal anomalies. It has been described in two siblings born to nonconsanguinous parents. The syndrome is lethal at birth (respiratory failure). Clinical manifestations include ear and facial a
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syndrome d'hypoplasie péroné-cubitus-anomalies rénales
SNOMEDCT-BE (respiratory failure). Clinical manifestations include ear and facial a / 716094008
SNOMEDCT-BE (disorder) / 716094008
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https://browser.ihtsdotools.or (...) [HTML]
A newly described syndrome associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations. Eight cases have been reported to date. The most common facial features include eye anom
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syndrome de microdélétion 6p22
SNOMEDCT-BE (disorder) / 719662000
SNOMEDCT-BE (disorder) / 719662000
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https://browser.ihtsdotools.or (...) [HTML]
A multiple developmental anomalies syndrome with characteristics of neurological abnormalities (including megalencephaly, hypotonia, intellectual disability, abnormal EEG), dysmorphic facial features (high prominent forehead, grooved nasal tip, ptosi
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syndrome neuro-facio-digito-rénal
SNOMEDCT-BE (including megalencephaly, hypotonia, intellectual disability, abnormal EEG), dysmorphic facial features (high prominent forehead, grooved nasal tip, ptosi / 725908007
SNOMEDCT-BE (disorder) / 725908007
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https://browser.ihtsdotools.or (...) [HTML]
A rare multiple malformation syndrome with characteristics of severe intrauterine growth retardation, severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. Severe central nervous system defects
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syndrome de Neu-Laxova
SNOMEDCT-BE (collodion baby type), and facial dysmorphism. Severe central nervous system defects / 77817004
SNOMEDCT-BE (disorder) / 77817004
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https://browser.ihtsdotools.or (...) [HTML]


Others have searched : eosinophilic granuloma    granuloma faciale    granuloma pyogenicum    verrucous xanthoma    eosinophilic granuloma of skin    oral mucosa    


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'granuloma faciale'

Date index:2021-10-26 -

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