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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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TPNH-Methemoglobin reductase deficiency
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C563171 |
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van den bosch syndrome
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C563129 |
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von Willebrand disease type 2N
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15631 |
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sensitive to dexamethasone aldosteronism
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C563177 |
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von Willebrand disease, type 2N
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15631 |
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von Willebrand disease Normandy variant
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15631 |
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COD (cerebroocular dysgenesis)
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C535631 |
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x-linked spondylometaphyseal dysplasia
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C563124 |
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Madura foot due to Actinomadura
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5631 |
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bleeding abnormality due to deficiency of platelet binding of factor x
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C563120 |
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anaerobic Actinomyces infection
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5631 |
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hyperhidrosis palmaris et plantaris
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C563185 |
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familial, type i hyperaldosteronism
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C563177 |
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histiocytoma, angiomatoid fibrous
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C563181 |
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double inguinal hernia
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C563164 |
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