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Det sätt begreppsrelationer visas:
Amelogenesis imperfecta
Hierarki: | ∟ ∟ ∟ ∟ ∟ Amelogenesis imperfecta 7 sidobegrepp1 underordnad begrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Amelogenesis imperfecta 7 sidobegrepp1 underordnad begrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Amelogenesis imperfecta 7 sidobegrepp1 underordnad begrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Bredare villkor: | |
Snävare villkor: | |
Anmärkning: | An autosomal dominant or X-linked disorder in which there is faulty development of the dental enamel owing to agenesis, hypoplasia, or hypocalcification of the enamel. It is marked by enamel that is very thin and friable and frequently stained in various shades of brown. (Dorland, 27th ed)
X |
Annotation: | a tooth abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
X |
historyNote*: | 65
X |
publicMeSHNote*: | 65
X |
activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1965-01-01X |
dateRevised*: | 1999-11-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | kleX |
recordOriginator*: | NLMX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Epätäydellinen kiilteenmuodostus (fi, ersatt) XAmelogenesis imperfecta (la-FI, ersatt) |
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