Disease Browser
Parent Node: Tooth Abnormalities (D014071) ..Starting node .. Odontodysplasia (D018126) Child Nodes:
........Odontoonychodermal dysplasia (C537742) ........Singleton Merten syndrome (C537343) ........Trichodental syndrome (C536551) Sister Nodes: ..Ackerman syndrome (C538170) ..Anodontia (D000848) 29 ..AREDYLD Syndrome (C537427) ..Blepharo-cheilo-dontic syndrome (C536188) ..Book Syndrome (C562993) ..Carabelli Anomaly of Maxillary Molar Teeth (C566175) ..Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only (C563974) ..CODAS syndrome (C536434) ..Deafness with Labyrinthine Aplasia Microtia and Microdontia (LAMM) (C548011) ..Deafness, Congenital, and Onychodystrophy, Autosomal Dominant (C567274) ..Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia (C565195) ..Dens in Dente (D003719) 1 ..Dental Enamel Hypoplasia (D003744) 29 ..Dentin Dysplasia (D003805) 3 ..Dentinogenesis Imperfecta (D003811) 7 ..Dermoodontodysplasia (C565103) ..Diastema, Dental Medial (C565098) ..Euhidrotic ectodermal dysplasia (C535763) ..Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification (C567039) ..Faciocardiomelic Dysplasia, Lethal (C565578) ..Fused Teeth (D005671) ..Grubben de Cock Borghgraef syndrome (C537621) ..Hypoglossia-Hypodactylia (C566308) ..Iridogoniodysgenesis, dominant type (C535536) ..Kallmann Syndrome 2 with Selective Tooth Agenesis (C566948) ..KBG syndrome (C537015) ..Lacrimoauriculodentodigital syndrome (C538132) ..Larsen syndrome, dominant type (C537873) ..Nance-Horan syndrome (C538336) ..Oculodentodigital Dysplasia (C563160) ..Oculodentodigital Dysplasia, Autosomal Recessive (C567605) ..Oculotrichodysplasia (C564934) ..Odontodysplasia (D018126) 3 ..Odontomicronychial dysplasia (C537741) ..Odontotrichoungual-Digital-Palmar Syndrome (C566598) ..Oroacral Syndrome, Verloes-Koulischer Type (C566374) ..Otodental Dysplasia (C563482) ..Polydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880) ..Rodrigues blindness (C535865) ..Spondyloepimetaphyseal Dysplasia With Abnormal Dentition (C566644) ..Taurodontism (C536946) ..Taurodontism, microdontia, and dens invaginatus (C536947) ..Teeth noneruption of with maxillary hypoplasia and genu valgum (C536952) ..Teeth, Odd Shapes Of (C566076) ..Temtamy preaxial brachydactyly syndrome (C536958) ..Tooth Agenesis, Selective, 2 (C566513) ..Tooth Agenesis, Selective, 3 (C567036) ..Tooth Agenesis, Selective, 4 (C563634) ..Tooth Agenesis, Selective, 5 (C565757) ..Tooth Agenesis, Selective, 6 (C567755) ..Tooth Agenesis, Selective, X-Linked, 1 (C567060) ..Tooth, Supernumerary (D014096) 3 ..Tricho-dento-osseous syndrome 1 (C536550) ..TRICHODENTOOSSEOUS SYNDROME (OMIM:190320) ..Weyers acrofacial dysostosis (C536695) ..Zazam Sheriff Phillips syndrome (C536723) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 8199
Name: Odontodysplasia
Definition: A localized arrested tooth development which appears to involve most commonly the anterior teeth, usually on one side of the midline, most often the maxillary central and lateral incisors. Roentgenographically, the teeth have a ghostlike appearance. Calcification and bits of prismatic enamel may be found in the pulp and the enamel is thin and absent in part. (Jablonski, Illustrated Dictionary of Dentistry, 1982)
Alternative IDs:
ParentIDs: MESH:D014071
TreeNumbers: C07.650.800.600 |C07.793.700.600 |C16.131.850.800.600
Synonyms: Dysplasia, Odontogenic |Dysplasias, Odontogenic |Ghost Teeth |Ghost Tooth |Odontodysplasias |Odontogenesis Imperfecta |Odontogenic Dysplasia |Odontogenic Dysplasias |Teeth, Ghost |Tooth, Ghost
Slim Mappings: Congenital abnormality|Mouth disease
Reference:
MedGen: D018126
MeSH: D018126
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants