Rare – Page 591 – CheckOrphan

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Microcephaly with chorioretinopathy- autosomal dominant form

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Microcephaly sparse hair mental retardation seizures

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Microcoria- congenital

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Microcephaly- hiatal hernia and nephrotic syndrome

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Microcephaly- corpus callosum dysgenesis and cleft lip-palate

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Microcephaly- primary autosomal recessive

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Microcephaly- holoprosencephaly- and intrauterine growth retardation

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Microcornea corectopia macular hypoplasia

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MED 23 gene defect

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Moersch-Woltman Condition

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