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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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spondylometaphyseal dysplasia, richmond type
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C563124 |
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x-linked 1 spinocerebellar ataxia
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C563134 |
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richmond type spondylometaphyseal dysplasia
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C563124 |
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ACTH-Dependent hyperaldosteronism syndrome
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C563177 |
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oral-facial-digital syndrome, type VII
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C563104 |
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hyperaldosteronism, familial, type i
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C563177 |
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agenesis of, with abnormal genitalia corpus callosum
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C563110 |
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agenesis of, with facial anomalies and robin sequence corpus callosum
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C563127 |
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autosomal dominant wolfram-like syndrome
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C565631 |
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spondylometaphyseal dysplasia, x-linked
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C563124 |
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olivopontocerebellar atrophy, x-linked
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C563134 |
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spinocerebellar ataxia, x-linked 1
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C563134 |
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mental retardation, x-linked 16
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C563139 |
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mental retardation, x-linked 17
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C563140 |
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mental retardation, x-linked 19
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C563141 |
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