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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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corpus callosum, agenesis of, with Facial anomalies and cerebellar ataxia
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14787 |
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infantile periodic alternating nystagmus 5
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C564478 |
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infantile periodic alternating, x-linked nystagmus
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C564478 |
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hemorrhagic fever, american
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D006478 |
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nasal cavity and paranasal sinus squamous cell cancer
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44787 |
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nasal cavity and paranasal sinus squamous cell carcinoma
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44787 |
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odontogenic keratocysts, and skeletal anomalies multiple basal cell nevi
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D001478 |
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hemorrhagic fever, argentinian
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D006478 |
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Kenny-Caffey syndrome, autosomal dominant
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7478 |
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hyper-IgE syndrome, autosomal recessive
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9478 |
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nevus syndrome, basal cell
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D001478 |
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nasopharyngeal neoplasm, benign
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21478 |
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inflammation of biliary tree
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4789 |
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hemorrhagic fever, bolivian
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D006478 |
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solid Papillary breast carcinoma
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44783 |
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