Disease Browser
Parent Node: Tooth Abnormalities (D014071) ..Starting node .. Fused Teeth (D005671) Child Nodes:
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: 4466
Name: Fused Teeth
Definition: Two teeth united during development by the union of their tooth germs; the teeth may be joined by the enamel of their crowns, by their root dentin, or by both.
Alternative IDs:
ParentIDs: MESH:D014071
TreeNumbers: C07.650.800.370 |C07.793.700.370 |C16.131.850.800.370
Synonyms: Double Tooth |Double Tooths |Fused Mandibular Incisor |Fused Mandibular Incisors |Incisor, Fused Mandibular |Incisors, Fused Mandibular |Mandibular Incisor, Fused |Mandibular Incisors, Fused |Teeth, Fused |Tooth, Double |Tooths, Double
Slim Mappings: Congenital abnormality|Mouth disease
Reference:
MedGen: D005671
MeSH: D005671
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants