Visningssätt för begreppens/termernas förhållanden:
Det sätt begreppsrelationer visas:
Det sätt begreppsrelationer visas:
Mandibulofacial dysostos
Hierarki: | ∟ ∟ ∟ ∟ ∟ ∟ Mandibulofacial dysostos 2 sidobegrepp1 underordnad begrepp∟ ∟ ∟ ∟ ∟ Mandibulofacial dysostos 2 sidobegrepp1 underordnad begrepp∟ ∟ ∟ ∟ ∟ ∟ Mandibulofacial dysostos 2 sidobegrepp1 underordnad begreppX |
Bredare villkor: | |
Snävare villkor: | |
Anmärkning: | A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)
X |
Annotation: | a form of craniofacial dysostosis; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
X |
activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | agsX |
recordOriginator*: | NLMX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Mandibulofasiaalinen dysostoosi (fi) XTreacher Collinsin syndrooma (fi, ersatt) Treacher Collinsin oireyhtymä (fi, ersatt) Franseschettin oireyhtymä (fi, ersatt) Franseschettin syndrooma (fi, ersatt) Treacher Collins syndrom (sv, ersatt) Mandibulofacial Dysostosis (en) Treacher Collins Syndrome (en, ersatt) Dysostosis mandibulofacialis (la-FI, ersatt) |
Dela: |
Laddar resultat...