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Oculogastrointestinal-neurodevelopmental syndrome

MONDO:0036189

Also known as: OGIN Syndrome

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

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Part of

↑ Hereditary disease (18187) ↑ Syndromic disease (7133)
Including sub-types (0) Tagged with Oculogastrointestinal-neurodevelopmental syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.