ONKI3 | Medical Subject Headings

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Dental Enamel Hypoplasia

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta ∟ Dental Enamel Hypoplasia Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta ∟ Dental Enamel Hypoplasia Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Tooth Diseases ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta ∟ Dental Enamel Hypoplasia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta ∟ Dental Enamel Hypoplasia Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Stomatognathic System Abnormalities ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta ∟ Dental Enamel Hypoplasia Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Tooth Diseases ∟ Tooth Abnormalities ∟ Amelogenesis Imperfecta ∟ Dental Enamel Hypoplasia Amelogenesis Imperfecta > Tooth Abnormalities > Stomatognathic System Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Amelogenesis Imperfecta > Tooth Abnormalities > Stomatognathic System Abnormalities > Stomatognathic Diseases > Medical Subject Headings (MeSH) Amelogenesis Imperfecta > Tooth Abnormalities > Tooth Diseases > Stomatognathic Diseases > Medical Subject Headings (MeSH) X
Annotation:	a congen or acquired tooth abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; DF: DENT ENAMEL HYPOPLASIA X
historyNote*:	66; was ENAMEL HYPOPLASIA 1965 X
publicMeSHNote*:	66; was ENAMEL HYPOPLASIA 1965 X
Scope note:	A form of AMELOGENESIS IMPERFECTA characterized by incomplete formation of the dental enamel and transmitted as an X-linked or autosomal dominant trait. It is also associated with vitamin A, C, or D deficiency, infectious disease, prematurity, birth injury, Rh incompatibility, trauma, or local infection. Small grooves, pits, and fissures are seen in mild cases, deep horizontal rows of pits in severe cases, or absence of enamel in extreme cases. (Dorland, 27th ed) X
activeMeSHYear*:	2000 \| 2001 \| 2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1966-01-01X
dateRevised*:	1999-11-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	kleX
recordOriginator*:	NLMX
Type:	Concept X
URI:	X
Labels and equivalent concepts:	Kiillehypoplasia (fi) Hampaan kiillehypoplasia (fi, replaced) Hampaiden kiillehypoplasia (fi, replaced) Kiillehypoplasiat (fi, replaced) Hammaskiilteen hypoplasiat (fi, replaced) Hammaskiilteen hypoplasia (fi, replaced) Tandemaljhypoplasi (sv) Enamel Hypoplasia, Dental (en, replaced) Hypoplasia, Dental Enamel (en, replaced) Hypoplastic Enamel (en, replaced) Enamel Agenesis (en, replaced) X
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