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Pierre Robin Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ Pierre Robin Syndrome 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Pierre Robin Syndrome 4 coordinate concepts∟ ∟ ∟ ∟ Pierre Robin Syndrome 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Pierre Robin Syndrome 4 coordinate concepts∟ ∟ ∟ ∟ Pierre Robin Syndrome 4 coordinate concepts∟ ∟ ∟ ∟ ∟ Pierre Robin Syndrome 4 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ Pierre Robin Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Pierre Robin Syndrome ∟ ∟ ∟ ∟ Pierre Robin Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Pierre Robin Syndrome ∟ ∟ ∟ ∟ Pierre Robin Syndrome ∟ ∟ ∟ ∟ ∟ Pierre Robin Syndrome |
Annotation: | multiple oral abnorm; named for French dentist Pierre Robin: Robin is his surname; note: no hyphen; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
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historyNote*: | 65(64)
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publicMeSHNote*: | 65
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Scope note: | An autosomal recessive disorder characterized by brachygnathia and cleft palate, often associated with glossoptosis, backward and upward displacement of the larynx, and angulation of the manubrium sterni. Cleft palate makes sucking and swallowing difficult, permitting easy access of fluids into the larynx. It may appear in several syndromes or as an isolated hypoplasia. (Dorland, 27th ed)
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1965-01-01X |
dateRevised*: | 1999-11-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | kleX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Pierre Robinin oireyhtymä (fi) XRobinin oireyhtymä (fi, replaced) Robinin syndrooma (fi, replaced) Robinin assosiaatio (fi, replaced) Pierre Robinin syndrooma (fi, replaced) Pierre Robin -oireyhtymä (fi, replaced) Pierre Robin -syndrooma (fi, replaced) Pierre Robinin assosiaatio (fi, replaced) Pierre Robins syndrom (sv) Pierre-Robin Syndrome (en, replaced) Syndroma Pierre Robin (la-FI, replaced) |
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