ONKI3 | Medical Subject Headings

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Stomatognathic System Abnormalities ∟ Mouth Abnormalities ∟ Cleft Lip 8 coordinate concepts ∟ Cleft Palate \| ∟ Fibromatosis, Gingival \| ∟ Macrostomia \| ∟ Microstomia \| ∟ Velopharyngeal Insufficiency \| ∟ Cheilitis \| ∟ Herpes Labialis \| ∟ Lip Neoplasms Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Mouth Diseases ∟ Lip Diseases ∟ Cleft Lip 8 coordinate concepts ∟ Cleft Palate \| ∟ Fibromatosis, Gingival \| ∟ Macrostomia \| ∟ Microstomia \| ∟ Velopharyngeal Insufficiency \| ∟ Cheilitis \| ∟ Herpes Labialis \| ∟ Lip Neoplasms Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Mouth Diseases ∟ Mouth Abnormalities ∟ Cleft Lip 8 coordinate concepts ∟ Cleft Palate \| ∟ Fibromatosis, Gingival \| ∟ Macrostomia \| ∟ Microstomia \| ∟ Velopharyngeal Insufficiency \| ∟ Cheilitis \| ∟ Herpes Labialis \| ∟ Lip Neoplasms Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Stomatognathic System Abnormalities ∟ Mouth Abnormalities ∟ Cleft Lip 8 coordinate concepts ∟ Cleft Palate \| ∟ Fibromatosis, Gingival \| ∟ Macrostomia \| ∟ Microstomia \| ∟ Velopharyngeal Insufficiency \| ∟ Cheilitis \| ∟ Herpes Labialis \| ∟ Lip Neoplasms X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Stomatognathic System Abnormalities ∟ Mouth Abnormalities ∟ Cleft Lip Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Mouth Diseases ∟ Lip Diseases ∟ Cleft Lip Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Mouth Diseases ∟ Mouth Abnormalities ∟ Cleft Lip Medical Subject Headings (MeSH) ∟ Stomatognathic Diseases ∟ Stomatognathic System Abnormalities ∟ Mouth Abnormalities ∟ Cleft Lip Mouth Abnormalities > Stomatognathic System Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Lip Diseases > Mouth Diseases > Stomatognathic Diseases > Medical Subject Headings (MeSH) Mouth Abnormalities > Mouth Diseases > Stomatognathic Diseases > Medical Subject Headings (MeSH) Mouth Abnormalities > Stomatognathic System Abnormalities > Stomatognathic Diseases > Medical Subject Headings (MeSH) X
Annotation:	do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; when with CLEFT PALATE, do not also use ABNORMALITIES, MULTIPLE X
historyNote*:	65; was HARELIP 1963-64 X
publicMeSHNote*:	65; was HARELIP 1963-64 X
Scope note:	Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region. 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:	Cleft Palate \| Fibromatosis, Gingival \| Macrostomia \| Microstomia \| Velopharyngeal Insufficiency \| Cheilitis \| Herpes Labialis \| Lip Neoplasms X
URI:	X
Labels and equivalent concepts:	Huulihalkio (fi) Keiloskiisi (fi, replaced) Ristihuuli (fi, replaced) Läppspalt (sv) Harläpp (sv, replaced) Harmynthet (sv, replaced) Harelip (en, replaced) Labium fissum (la-FI, replaced) Cheiloschisis (la-FI, replaced) X
Share:	X