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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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presenile cataract foveal hypoplasia
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C537858 |
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fetal cystic hygroma
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C537852 |
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nystagmus 1, infantile, x-linked
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C537853 |
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posterior cleft larynx
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C537851 |
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congenital, x- linked nystagmus 1
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C537853 |
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fatty acid metabolism disorder
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37858 |
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nystagmus congenital, motor 2
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C537854 |
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nystagmus, congenital motor, 1
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C537853 |
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nystagmus, congenital motor, 2
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C537854 |
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autosomal recessive non-syndromic intellectual disability caused by mutation in CRADD
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13785 |
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congenital, x-linked nystagmus 1
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C537853 |
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infantile, x-linked nystagmus 1
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C537853 |
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motor 2 nystagmus congenital
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C537854 |
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CRADD autosomal recessive non-syndromic intellectual disability
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13785 |
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o'donnell pappas syndrome
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C537858 |
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