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Acrocephalosyndactylia
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate concept∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate concept∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate concept∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate concept∟ ∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate concept∟ ∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate concept∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate concept∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate concept∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate concept∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia 1 coordinate conceptX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia ∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia ∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia ∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia ∟ ∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia ∟ ∟ ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia ∟ ∟ ∟ ∟ ∟ Acrocephalosyndactylia |
Annotation: | congen deform of skull, fingers & toes; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
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Scope note: | Craniostenosis characterized by acrocephaly and syndactyly, probably occurring as an autosomal dominant trait and usually as a new mutation. (Dorland, 27th ed)
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 1999-11-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | kleX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Akrokefalosyndaktylia (fi) XPfeifferin syndrooma (fi, replaced) Apertin syndrooma (fi, replaced) Pfeifferin oireyhtymä (fi, replaced) Apertin oireyhtymä (fi, replaced) Akrocefalosyndaktyli (sv) Aperts syndrom (sv, replaced) Pfeiffers syndrom (sv, replaced) Saethre-Chotzens synrom (sv, replaced) Syndroma Apert (la-FI, replaced) |
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