About: tooth 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 teeth

Attributes	Values
rdf:type	Item
description	congenital absence of or defects in structures of the teeth (en)
exact match	wds:Q54912172-67F12CB5-8F0A-4469-ADE2-B5D16CE5B51A wds:Q54912172-D89BD83B-B446-4C36-A20C-B400DAB77E9B
exact match	http://purl.obolibrary.org/obo/DOID_702 http://purl.obolibrary.org/obo/HP_0000164
Disease Ontology ID	wds:Q54912172-5087EAF7-B172-4436-BF7D-3E0CA440E902
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:702
Disease Ontology ID	DOID:702
rdfs:label	anomalie dentaire congénitale (fr) anomalía dental (es) nepravilnost zob (sl) tooth abnormality (en) аномалия зуба (ru)
skos:prefLabel	anomalie dentaire congénitale (fr) anomalía dental (es) nepravilnost zob (sl) tooth abnormality (en) аномалия зуба (ru)
name	anomalie dentaire congénitale (fr) anomalía dental (es) nepravilnost zob (sl) tooth abnormality (en) аномалия зуба (ru)
instance of	wds:Q54912172-9f9b314b-4719-e4a4-a4af-300ba03a697e
instance of	medical finding
subclass of	wds:Q54912172-2c90685c-41a6-ddeb-8a5b-7420c0a8b909 wds:Q54912172-54f6fdc4-446b-df7d-ebc4-9de4bf5d6b3d wds:Q54912172-c9964cdb-4b65-16eb-d34f-69d1b505d4b8
subclass of	tooth pathology dentofacial deformity stomatognathic system abnormality
Human Phenotype Ontology ID	wds:Q54912172-A1B4FDCA-F6B9-44EE-9B55-476204E6DF03
Human Phenotype Ontology ID	HP:0000164
skos:altLabel	congenital dentition disorder (en) tooth abnormalities (en) zobna nepravilnost (sl)
UMLS CUI	wds:Q54912172-55E16710-C4AE-40CC-80D9-3C8D223723FA wds:Q54912172-69D80761-B46E-41F1-92FC-0B4F817140DD wds:Q54912172-AF15F441-39B8-4BC9-AF99-278DA46D43D4
MeSH descriptor ID	wds:Q54912172-B1F24269-CF43-4454-B419-895D5DAFCDB3
on focus list of Wikimedia project	wds:Q54912172-225625E7-3147-4506-8643-FB0C675B4E5F
MeSH tree code	wds:Q54912172-3dbc5ccb-4b86-1267-f139-cca12e521378 wds:Q54912172-ba802d35-409c-1c0c-9ea0-7bc82d6cdd02 wds:Q54912172-fcc1cf4e-47e6-adaa-d3ec-5666b34c6f33
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D014071
MeSH tree code	http://id.nlm.nih.gov/mesh/C07.650.800 http://id.nlm.nih.gov/mesh/C07.793.700 http://id.nlm.nih.gov/mesh/C16.131.850.800
UMLS CUI	C0040427 C0262444 C0524730
MeSH descriptor ID	D014071
on focus list of Wikimedia project	WikiProject Medicine
MeSH tree code	C07.650.800 C07.793.700 C16.131.850.800
is owl:sameAs of	tooth abnormality
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q54912172
is subclass of of	anodontia macrodontia Ectopic tooth tooth agenesis developmental defects of dental enamel
is subclass of of	wds:Q1923603-c04f18d4-4a34-bdb5-5cb5-eb9a8defa142 wds:Q116800674-fb59a42c-4d98-d1c4-d4a0-2290d6750730 wds:Q2719474-1b6b6637-443e-9a89-4dd7-b221affa22ed wds:Q771310-24b9a656-4135-41a1-9eb3-2cde1d6f4dbe wds:Q111913471-8b99a80e-4c0e-f831-b284-0769237ff509
is main subject of	TIME OF ERUPTION OF THE PERMANENT TEETH, CEPHALOMETRIC AND TOOTH MEASUREMENT AND SULPHATION FACTOR ACTIVITY IN 45 PATIENTS WITH TURNER'S SYNDROME WITH DIFFERENT TYPES OF X CHROMOSOME ABERRATIONS Oculo‐facio‐cardio‐dental syndrome: Skewed X chromosome inactivation in mother and daughter suggest X‐linked dominant Inheritance Globodontia--a new familial tooth abnormality Metabolic disturbances in tooth formation On the properties of the tooth eruption curve DWARFISM IN THE AMISH I. THE ELLIS-VAN CREVELD SYNDROME Multiple anomalies in dental morphology: Macrodontia, multituberculism, central cusps, and pulp invaginations Roentgen Differentiation of the Oculodentodigital Syndrome and the Hallermann-Streiff Syndrome in Infancy Odontodysplasia in the deciduous dentition Dental mutilation and associated abnormalities in Uganda Dental changes in osteopetrosis ULTRASONICS DIAGNOSIS OF MICROPHTHALMIA WITHOUT MICROCORNEA, WITH MACROPHAKIA, HIGH HYPERMETROPIA ASSOCIATED WITH TAPETO-RETINAL DEGENERATION, A GLAUCOMATOUS PREDISPOSITION AND DENTAL ANOMALIES (NEW FAMILIAL SYNDROME) Fusion of the incisor teeth of the maxillary and mandibular regions Evolution and dysmorphoses Incidence of the small dens in dente AVAILABLE SPACE FOR THE INCISORS DURING DENTAL DEVELOPMENT--A GROWTH STUDY BASED ON PHYSIOLOGIC AGE THE EFFECT OF PREMATURE LOSS OF DECIDUOUS MOLARS ON PREMOLAR ERUPTION GEMINATION, FUSION, TWINNING AND CONCRESCENCE Polyanomalodontia Dental abnormalities in the tricho-dento-osseous syndrome Incidence of Cervical Enamel Projections and its Relationship to Furcation Involvement in Egyptian Skulls Aberrant second premolars Talon cusp: a primary or a permanent incisor anomaly Taurodontism and concomitant hypodontia in siblings Congenital Malformations of Upper Incisors in Exencephalic Mouse Embryos, Induced by Hypervitaminosis a II. Morphology of Fused Upper Incisors Prenatal factors in oral pathologic conditions Dens invaginatus. Case report Radiological Changes in Teeth and Skull in Mental Defectives Objective registration of orthodontic anomalies Physical, histological and roentgenographic characteristics of the grey lethal mouse ABNORMAL MORPHOLOGY OF THE SOFT PALATE. II. THE GENETICS OF CLEFT UVULA

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