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The way concept relations are shown:
Craniofacial Dysostosis
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Craniofacial Dysostosis 14 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Craniofacial Dysostosis 14 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Craniofacial Dysostosis 14 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
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Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; "craniofacial dysmorphism" does not go here: index under FACIAL BONES /abnorm + SKULL /abnorm but not also under ABNORMALITIES, MULTIPLE
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Scope note: | An autosomal dominant disorder characterized by acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, and hypoplastic maxilla with relative mandibular prognathism. (Dorland, 27th ed)
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 1999-11-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | KEVX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Kraniofasiaalinen dysostoosi (fi) XCrouzonin tauti (fi, replaced) Crouzonin syndrooma (fi, replaced) Crouzonin oireyhtymä (fi, replaced) Kraniofacial dysostos (sv) Crouzons sjukdom (sv, replaced) Crouzon's Disease (en, replaced) Dysostosis, Craniofacial (en, replaced) Crouzon Disease (en, replaced) Dysostosis craniofacialis (la-FI, replaced) Morbus Crouzon (la-FI, replaced) Syndroma Crouzon (la-FI, replaced) |
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