autosomal dominant congenital deafness with onychodystrophy
blepharocheilodontic syndrome +
Book Syndrome
Carabelli Anomaly of Maxillary Molar Teeth
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 caries +
dental enamel hypoplasia +
An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors.
dentin dysplasia +
dentin sensitivity
dentinogenesis imperfecta +
Dermoodontodysplasia
DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES
Diastema +
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis
Euhidrotic Ectodermal Dysplasia
Fused Teeth
Grubben de Cock Borghgraef Syndrome
hypercementosis
Hypoglossia-Hypodactylia
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME
KBG syndrome
LADD syndrome +
Larsen syndrome
Lethal Faciocardiomelic Dysplasia
Nance-Horan syndrome
Noneruption of Teeth with Maxillary Hypoplasia and Genu Valgum
oculodentodigital dysplasia +
Oculoskeletodental Syndrome
Oculotrichodysplasia
Odd Shapes of Teeth
Odontodysplasia +
Odontomicronychial Dysplasia
Odontotrichoungual-Digital-Palmar Syndrome
Oroacral Syndrome, Verloes-Koulischer Type
Otodental Dysplasia
Postaxial Polydactyly, with Dental and Vertebral Anomalies
Rodrigues Blindness
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition