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| language |
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| license |
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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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deficiency, labile
|
9210 |
|
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hereditary hypoproaccelerinaemia
|
9210 |
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F7 deficiency
|
9211 |
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F10 deficiency
|
9212 |
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disease, Stuart-Prower
|
9212 |
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Fanconi Anemia
|
9215 |
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Bickel-Fanconi glycogenosis
|
9216 |
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Fanconi-Bickel disease
|
9216 |
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Fanconi-Bickel syndrome
|
9216 |
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GLUT2 deficiency
|
9216 |
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pseudo-phlorizin diabetes
|
9216 |
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Fanconi-like syndrome
|
9217 |
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AC deficiency
|
9218 |
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Farber disease
|
9218 |
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Farber lipogranulomatosis
|
9218 |
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