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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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neutral 17 beta-hydroxysteroid oxidoreductase deficiency
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C537805 |
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monosomy 6q1 chromosome 6
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C537808 |
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monosomy 6q2 chromosome 6
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C537809 |
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T lymphocyte deficiency
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3780 |
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17-hydroxysteroid dehydrogenase deficiency
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C537805 |
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18-alpha hydroxylase deficiency
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C537806 |
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CMO i deficiency
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C537806 |
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disorder of glycerol metabolic process
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37807 |
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17-beta hydroxysteroid dehydrogenase III deficiency
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C537805 |
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17 Beta-hydroxysteroid dehydrogenase deficiency
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C537805 |
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glycerol metabolism disease
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37807 |
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aldosterone deficiency due to defect in 18-hydroxylase
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C537806 |
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chromosome 10q duplication syndrome
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C537804 |
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male, with gynecomastia pseudohermaphroditism
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C537805 |
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hyperreninemic hypoaldosteronism, familial, type i
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C537806 |
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