Oculootodental syndrome

MONDO:0020494

Oculootodental 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

0 clinical trials for this condition and its sub-types, 0 tagged with Oculootodental syndrome itself.

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Part of

↑ Partial deletion of the long arm of chromosome 11 (0)

Including sub-types (0) Tagged with Oculootodental syndrome (0)

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