Rare – Page 42 – CheckOrphan

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Hoon Hall syndrome

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Hordnes Engebretsen Knudtson syndrome

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Homocystinuria due to defect in methylation- MTHFR deficiency

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Microtia- meatal atresia and conductive deafness

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Microtia- eye coloboma- and imperforation of the nasolacrimal duct

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Microvillus inclusion disease

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Microtia-Anotia

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Microsomia hemifacial radial defects

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Microscopic polyangiitis

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Microsporidiosis

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