mental retardation, autosomal recessive 34; MRT34
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http://purl.obolibrary.org/obo/MONDO_0013785 |
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intellectual disability, autosomal recessive type 34
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13785 |
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mental retardation, autosomal recessive type 34
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13785 |
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congenital, autosomal dominant nystagmus 2
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C537854 |
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White blood cell decreased
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3785 |
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nystagmus 1, congenital, x- linked
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C537853 |
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nystagmus 1, congenital, x-linked
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C537853 |
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congenital nystagmus, corneal pannus, and presenile cataracts foveal hypoplasia
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C537858 |
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congenital, autosomal dominant nystagmus 3
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C537855 |
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congenital, autosomal dominant nystagmus 4
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C537856 |
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familial, 2, due to red cell leak pseudohyperkalemia
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C563785 |
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autosomal recessive non-syndromic intellectual disability caused by mutation in CRADD
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13785 |
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presenile cataract foveal hypoplasia
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C537858 |
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