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Hallermann's Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ Hallermann's Syndrome 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Hallermann's Syndrome 2 coordinate concepts∟ ∟ ∟ ∟ ∟ Hallermann's Syndrome 2 coordinate conceptsX |
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Annotation: | a form of craniofacial dysostosis with other abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
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historyNote*: | 91(65); was see under CRANIOFACIAL DYSOSTOSIS 1985-90; was see under MANDIBULOFACIAL DYSOSTOSIS 1965-84
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publicMeSHNote*: | 91; was see under CRANIOFACIAL DYSOSTOSIS 1985-90; was see under MANDIBULOFACIAL DYSOSTOSIS 1965-84
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Scope note: | An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed)
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 1999-11-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | kleX |
recordOriginator*: | NLMX |
Type: | |
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URI: | |
Labels and equivalent concepts: | Hallermann-Streiffin oireyhtymä (fi) XOkulomandibulofasiaalinen oireyhtymä (fi, replaced) Hallermannin syndrooma (fi, replaced) Hallermannin oireyhtymä (fi, replaced) Hallermann-Streiffin syndrooma (fi, replaced) Hallermanns syndrom (sv) Hallermann-Streiff Syndrome (en, replaced) Syndroma Hallermann (la-FI, replaced) |
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