Rare – Page 234 – CheckOrphan

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Iridogoniodysgenesis and skeletal anomalies

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Iridogoniodysgenesis type1

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Iridogoniodysgenesis- dominant type

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Iris dysplasia hypertelorism deafness

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Iris hypoplasia and glaucoma

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Maternally Inherited Leigh Syndrome

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Mastocytosis- cutaneous- with short stature- conductive hearing loss and microtia

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Mastocytic enterocolitis

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Mast Cell Disease

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Mathieu De Broca Bony syndrome

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