ONKI3 | Medical Subject Headings

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Dentinogenesis Imperfecta

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Dentinogenesis Imperfecta 7 coordinate concepts ∟ Amelogenesis Imperfecta \| ∟ Anodontia \| ∟ Dens in Dente \| ∟ Dentin Dysplasia \| ∟ Fused Teeth \| ∟ Odontodysplasia \| ∟ Tooth, Supernumerary Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Dentinogenesis Imperfecta 7 coordinate concepts ∟ Amelogenesis Imperfecta \| ∟ Anodontia \| ∟ Dens in Dente \| ∟ Dentin Dysplasia \| ∟ Fused Teeth \| ∟ Odontodysplasia \| ∟ Tooth, Supernumerary Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Tooth Diseases ∟ Tooth Abnormalities ∟ Dentinogenesis Imperfecta 7 coordinate concepts ∟ Amelogenesis Imperfecta \| ∟ Anodontia \| ∟ Dens in Dente \| ∟ Dentin Dysplasia \| ∟ Fused Teeth \| ∟ Odontodysplasia \| ∟ Tooth, Supernumerary X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Dentinogenesis Imperfecta Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Dentinogenesis Imperfecta Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Tooth Diseases ∟ Tooth Abnormalities ∟ Dentinogenesis Imperfecta Tooth Abnormalities > Stomatognathic System Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Tooth Abnormalities > Stomatognathic System Abnormalities > Stomatognathic Diseases > Medical Subject Headings (MeSH) Tooth Abnormalities > Tooth Diseases > Stomatognathic Diseases > Medical Subject Headings (MeSH) X
Annotation:	a dentin abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
historyNote*:	65 X
publicMeSHNote*:	65 X
Scope note:	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) X
activeMeSHYear*:	2000 \| 2001 \| 2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	1999-11-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	kleX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Amelogenesis Imperfecta \| Anodontia \| Dens in Dente \| Dentin Dysplasia \| Fused Teeth \| Odontodysplasia \| Tooth, Supernumerary X
URI:	X
Share:	X