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Tandemaljhypoplasi
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Anmärkning: | A form of AMELOGENESIS IMPERFECTA characterized by incomplete formation of the dental enamel and transmitted as an X-linked or autosomal dominant trait. It is also associated with vitamin A, C, or D deficiency, infectious disease, prematurity, birth injury, Rh incompatibility, trauma, or local infection. Small grooves, pits, and fissures are seen in mild cases, deep horizontal rows of pits in severe cases, or absence of enamel in extreme cases. (Dorland, 27th ed)
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Annotation: | a congen or acquired tooth abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; DF: DENT ENAMEL HYPOPLASIA
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historyNote*: | 66; was ENAMEL HYPOPLASIA 1965
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publicMeSHNote*: | 66; was ENAMEL HYPOPLASIA 1965
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1966-01-01X |
dateRevised*: | 1999-11-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | kleX |
recordOriginator*: | NLMX |
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Termer och motsvarande begrepp: | Kiillehypoplasia (fi) XHampaan kiillehypoplasia (fi, ersatt) Hampaiden kiillehypoplasia (fi, ersatt) Kiillehypoplasiat (fi, ersatt) Hammaskiilteen hypoplasiat (fi, ersatt) Hammaskiilteen hypoplasia (fi, ersatt) Dental Enamel Hypoplasia (en) Enamel Hypoplasia, Dental (en, ersatt) Hypoplasia, Dental Enamel (en, ersatt) Hypoplastic Enamel (en, ersatt) Enamel Agenesis (en, ersatt) |
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