autosomal dominant congenital deafness with onychodystrophy
blepharocheilodontic syndrome +
Book Syndrome
Bork Stender Schmidt Syndrome
bruxism +
Carabelli Anomaly of Maxillary Molar Teeth
cerebellofaciodental syndrome
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only
CODAS syndrome
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia
Craniosynostosis and Dental Anomalies
Dens in Dente +
dental abscess
Dental Deposits +
dental enamel hypoplasia +
dental fluorosis
Dental Leakage
dental pulp disease +
dentin dysplasia +
dentin sensitivity
dentinogenesis imperfecta +
An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated.
Dermoodontodysplasia
DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES
Diastema +
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis
Edentulous Mouth +
Euhidrotic Ectodermal Dysplasia
Focal Infection, Dental
Fused Teeth
Grubben de Cock Borghgraef Syndrome
Hypoglossia-Hypodactylia
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME
KBG syndrome
LADD syndrome
Larsen syndrome
Lethal Faciocardiomelic Dysplasia
Malocclusion +
Nance-Horan syndrome
oculodentodigital dysplasia +
Oculoskeletodental Syndrome
Oculotrichodysplasia
Odd Shapes of Teeth
Odontodysplasia +
Odontomicronychial Dysplasia
Odontotrichoungual-Digital-Palmar Syndrome
Oroacral Syndrome, Verloes-Koulischer Type
Otodental Dysplasia
periodontal disease +
Postaxial Polydactyly, with Dental and Vertebral Anomalies
primary failure of tooth eruption
Rodrigues Blindness
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition
Supernumerary Tooth +
Taurodontism +
Taurodontism, Microdontia, and Dens Invaginatus
teeth hard tissue disease +
Teeth Noneruption of with Maxillary Hypoplasia and Genu Valgum