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Oculootodental syndrome
MONDO:0020494Oculootodental syndrome is a contiguous gene syndrome comprising otodental syndrome (characterized by globodontia and sensorineural high-frequency hearing deficit) associated with eye abnormalities including, typically, iris and chorioretinal coloboma, as well as, on occasion, microcornea, microphtalmos, lenticular opacity, lens coloboma and iris pigment epithelial atrophy.
Also known as: OOD
2 clinical trials for this condition and its sub-types.
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Disease
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Human disease
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Chromosomal disorder
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Disease of genetic or genomic mechanism
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Autosomal anomaly
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Chromosome 11 disorder
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Disease by etiologic mechanism
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Partial deletion of chromosome 11
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Partial deletion of the long arm of chromosome 11
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Syndrome caused by partial chromosomal deletion
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