Oculootodental syndrome

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Synonyms: OOD

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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version July 2024

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Oculootodental syndrome?

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Clinical Trials

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