ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Amelogenesis Imperfecta

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta 7 coordinate concepts 1 subordinate concept ∟ Dental Enamel Hypoplasia ∟ Anodontia \| ∟ Dens in Dente \| ∟ Dentin Dysplasia \| ∟ Dentinogenesis Imperfecta \| ∟ Fused Teeth \| ∟ Odontodysplasia \| ∟ Tooth, Supernumerary Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta 7 coordinate concepts 1 subordinate concept ∟ Dental Enamel Hypoplasia ∟ Anodontia \| ∟ Dens in Dente \| ∟ Dentin Dysplasia \| ∟ Dentinogenesis Imperfecta \| ∟ Fused Teeth \| ∟ Odontodysplasia \| ∟ Tooth, Supernumerary Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Tooth Diseases ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta 7 coordinate concepts 1 subordinate concept ∟ Dental Enamel Hypoplasia ∟ Anodontia \| ∟ Dens in Dente \| ∟ Dentin Dysplasia \| ∟ Dentinogenesis Imperfecta \| ∟ 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 ∟ Amelogenesis Imperfecta Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Tooth Diseases ∟ Tooth Abnormalities ∟ Amelogenesis 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
Narrower terms:	Dental Enamel Hypoplasia X
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 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
activeMeSHYear*:	2000 \| 2001 \| 2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1965-01-01X
dateRevised*:	1999-11-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	kleX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Anodontia \| Dens in Dente \| Dentin Dysplasia \| Dentinogenesis Imperfecta \| Fused Teeth \| Odontodysplasia \| Tooth, Supernumerary X
URI:	X
Labels and equivalent concepts:	Epätäydellinen kiilteenmuodostus (fi, replaced) Amelogenesis imperfecta (la-FI, replaced) X
Share:	X