Rare – Page 370 – CheckOrphan

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Larsen syndrome- dominant type

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Epiphyseal dysplasia dysmorphism camptodactyly

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Epiphyseal dysplasia hearing loss dysmorphism

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Nystagmus- congenital motor- autosomal recessive

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Nystagmus- hereditary vertical

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Novak syndrome

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Nuchal bleb- familial

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Nystagmus 1- congenital- X- linked

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Epimetaphyseal skeletal dysplasia

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Tricho-dento-osseous syndrome 1

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