oculootodental syndrome
MONDO:0020494Mondo
Findings
No curated finding names oculootodental syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0020494), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
1 name
Resolves to: oculootodental syndrome
- Also called
- OOD