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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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gorham-stout disease
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D010015 |
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gorhams disease
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D010015 |
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massive osteolyses
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D010015 |
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osteolyses, essential
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D010015 |
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osteolysis, essential
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D010015 |
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corneal opacification and other ocular anomalies
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10015 |
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megaloblastic anemia, 1
|
100156 |
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Abderhalden Lignac Kaufmann disease
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100151 |
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Abderhalden Kaufmann Lignac syndrome
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100151 |
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diffuse cystic angiomatosis of bone
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D010015 |
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megaloblastic anemia, Norwegian type
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100157 |
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sclerocornea with Other ocular anomalies
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10015 |
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megaloblastic anemia, Finnish type
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100156 |
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gorham stout disease
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D010015 |
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PXDN anterior segment dysgenesis
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10015 |
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