The way property values are displayed:
The way concept relations are shown:
The way concept relations are shown:
Dentin Dysplasia
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Dentin Dysplasia 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Dentin Dysplasia 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Dentin Dysplasia 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | |
Annotation: | a tooth abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
X |
historyNote*: | 65
X |
publicMeSHNote*: | 65
X |
Scope note: | An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed)
X |
activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1965-01-01X |
dateRevised*: | 1999-11-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | kleX |
recordOriginator*: | NLMX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Dentiinidysplasia (fi) XHammasluun dysplasia (fi, replaced) Dentiinin dysplasia (fi, replaced) Dentindysplasi (sv) Dysplasia dentinalis (la-FI, replaced) |
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