About: mouth abnormality

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

congenital absence of or defects in structures of the mouth

Attributes	Values
rdf:type	Item
description	congenital absence of or defects in structures of the mouth (en)
exact match	wds:Q54931797-206E466E-7857-492C-8F82-0BF2B89183A0
exact match	http://purl.obolibrary.org/obo/HP_0000153
health specialty	wds:Q54931797-22042515-A08B-4158-827E-9136EEB2D138
ICD-10	wds:Q54931797-2d044dd6-48ba-088e-c9c9-ad52ef44e9c9
health specialty	Oral and maxillofacial surgery
ICD-10	Q38.6
rdfs:label	malformation de la bouche (fr) mouth abnormality (en) mutes anomālija (lv)
skos:prefLabel	malformation de la bouche (fr) mouth abnormality (en) mutes anomālija (lv)
name	malformation de la bouche (fr) mouth abnormality (en) mutes anomālija (lv)
instance of	wds:Q54931797-a3c6fa0b-4ab9-1a74-35ef-ef7278062be0
instance of	disease
subclass of	wds:Q54931797-5fb43b8d-4f6d-c7f3-31ef-7835675c0739 wds:Q54931797-852a3d90-4a9b-a5b9-e97c-1ef19343ed2d wds:Q54931797-ad1898e4-4649-d528-4bc2-1e9c683f7de3
subclass of	craniofacial abnormality mouth disease stomatognathic system abnormality
Medical Dictionary...ory Activities ID	wds:Q54931797-863B2115-BC7C-407C-BF54-88A00CD74F5D
Human Phenotype Ontology ID	wds:Q54931797-C50694BE-DCCB-4B66-AF0D-E0C409AA13DB
Medical Dictionary...ory Activities ID	http://purl.bioontology.org/ontology/MDRFRE/10061070
Medical Dictionary...ory Activities ID	10061070
Human Phenotype Ontology ID	HP:0000153
skos:altLabel	mouth abnormalities (en)
National Library of Latvia ID	wds:Q54931797-2e49efb7-4095-5abb-dafc-8f33f41e10f8
UMLS CUI	wds:Q54931797-19E1FF82-4499-4194-9947-9D735E519476
MeSH descriptor ID	wds:Q54931797-C30A3450-E64F-4146-B579-E58875D65461
MeSH tree code	wds:Q54931797-9012CBC7-EF57-485E-BDAE-CBAE3764BEF5 wds:Q54931797-AEE588B9-BCDA-4916-88BB-A61EEF63C055 wds:Q54931797-C678223F-A470-4ACF-BE65-B288930ACC63
topic's main category	wds:Q54931797-4e52909f-492d-14e2-bf80-dad14490803b
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D009056
MeSH tree code	http://id.nlm.nih.gov/mesh/C07.465.525 http://id.nlm.nih.gov/mesh/C07.650.525 http://id.nlm.nih.gov/mesh/C16.131.850.525
National Library of Latvia ID	000320249
UMLS CUI	C0026633
MeSH descriptor ID	D009056
MeSH tree code	C07.465.525 C07.650.525 C16.131.850.525
topic's main category	Category:Congenital oral disorders
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q54931797
is main subject of	The oral manifestations of Apert syndrome The oral-facial-digital syndrome: a multiple congenital condition of females with associated chromosomal abnormalities The teratogenic effects of hypervitaminosis A upon the face and mouth of inbred mice Mortality and skeletal malformations from amniocentesis and oligohydramnios in rats: Cleft palate, clubfoot, microstomia, and adactyly Nosologic and genetic considerations in the aglossy-adactyly syndrome CONGENITAL MALFORMATIONS IN MYOTONIC DYSTROPHY TONGUE TIE Epidemiologic studies of oral anomalies and diseases in the Department at Antioquia. IV. Pupils of Entrerrios Prenatal factors in oral pathologic conditions PALATAL AND MANDIBULAR TORI IN THE NEGRO BILATERAL HYPERTROPHY OF MENTAL TUBERCLES. A CASE REPORT Oculovertebral Syndrome Dental involvement of an infant with Potter syndrome: case report SURGICAL CORRECTION OF MAXILLOMANDIBULAR DEFORMITIES Clefts of the cheek in the place of the first branchial cleft WHAT THE DOCTOR SHOULD KNOW ABOUT ORAL PATHOLOGY Orofacial signs and dental abnormalities in patients with Mulvihill-Smith syndrome: A literature review on this rare progeroid pathology ON THE PREVENTION AND EARLY TREATMENT OF DYSGNATHIA Partial Oral Duplication: A Defect in Ectomesenchymal Migration? Lingual leiomyomatous hamartoma with bifid tip and ankyloglossia in a patient without oral-facial-digital syndrome: a case report and literature review Persistent buccopharyngeal membrane. Case report Goldenhar’s Syndrome, Oculo-Auricular Malformation, in a Bantu Girl PROSTHETIC CARE OF FACIAL AND ORAL DEFECTS Some craniofacial anomalies CONGENITAL MALFORMATIONS. CLINICAL AND COMMUNITY CONSIDERATIONS On a rare case of dysembryoplasia localized in the face and the hand FIBROUS DYSPLASIA OF BONE WITH OTHER DEVELOPMENTAL ANOMALIES: REPORT OF CASE Hypopituitarism associated with cystic Rathke's cleft in a dog Epidemiologic studies of oral anomalies and diseases in the Department at Antioquia. I. Pupils of Bolivar Epidemiologic studies of oral anomalies and diseases in the Department at Antioquia. III. Katio Indian pupils of Dabeiba Split denture for patients unable to 'open wide' THE IMPORTANCE OF NOTING MINOR MALFORMATIONS SUCH AS FOVEOLAE ANGULI ORIS ("MUNDWINKELGRUEBCHEN"). A BRIEF CONTRIBUTION TO TOPOGRAPHIC DERMATOLOGY Neighborhood Deprivation and Risk of Congenital Heart Defects, Neural Tube Defects and Orofacial Clefts: A Systematic Review and Meta-Analysis TORUS MANDIBULARIS: A GENETICS STUDY Multiple congenital abnormalities with diaphyseal dysplasia (Camurati—Engelmann's syndrome) Choanol imperforation in the newborn Certain aspects of mouth pathology in children Dento-labial dysplasias, a syndrome of the primary oral epithelium Congenital intermaxillary fibrous bands MULTIDISCIPLINARY DIAGNOSIS AND TREATMENT PLANNING FOR THE PATIENT WITH DENTAL-FACIAL ABNORMALITIES Construction of a complete upper and lower prosthesis in cases of microstomia Nasotracheal intubation with the aid of lateral roentgenoscopy of the neck in patients with congenital and acquired defects and deformities of the maxillofacial region Enzymes and enzymopathies in odontology Oropalatal band (maxillo-mandibular band). off Special prosthoelontic methods for patients with microstomia TONGUE-MOUTH-CHEEK BEHAVIOR IN VARIOUS DYSMORPHOSES AND THEIR CORRECTION USING BALTERS' FUNCTIONAL APPARATUS Letter: Asymetry of the mouth during crying Problem of developmental anomalies in otorhinolaryngology Epidemiologic studies of oral anomalies and diseases in the Department at Antioquia. II. Pupils of Dabeiba Epidemiologic studies of oral anomalies and diseases in the Department at Antioquia. V. Summary and conclusions: the 9 most frequent lesions in 883 Antioqueno pupils

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