Otodental syndrome
MONDO:0008161Otodental syndrome is a very rare inherited condition characterized by grossly enlarged canine and molar teeth (globodontia) associated with sensorineural hearing loss.
Also known as: globodontia, otodental dysplasia, otodental dysplasia chromosome deletion syndrome, otodental syndrome, chromosome 11q13 deletion syndrome, oculootodental syndrome, otodental syndrome with coloboma
0 clinical trials for this condition and its sub-types.
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Disease
(680)
Human disease
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
(0)
Chromosome 11 disorder
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
Disorder of development or morphogenesis
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Partial deletion of chromosome 11
(0)
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