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Det sätt begreppsrelationer visas:
Dentinogenesis imperfecta
Hierarki: | ∟ ∟ ∟ ∟ ∟ Dentinogenesis imperfecta 7 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Dentinogenesis imperfecta 7 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Dentinogenesis imperfecta 7 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Bredare villkor: | |
Anmärkning: | An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth, ranging from dusky blue to brownish. The dentin is poorly formed with an abnormally low mineral content; the pulp canal is obliterated, but the enamel is normal. The teeth usually wear down rapidly, leaving short, brown stumps. (Dorland, 27th ed)
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Annotation: | a dentin abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
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historyNote*: | 65
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publicMeSHNote*: | 65
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 1999-11-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | kleX |
recordOriginator*: | NLMX |
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