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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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Huntington disease-like 4
|
11781 |
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systemic Immunoglobulin Light chain amyloidosis
|
17816 |
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Van Maldergem Wetzburger Verloes syndrome
|
17813 |
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uterine corpus adenomatoid tumor
|
1781 |
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variant ABeta2M amyloidosis
|
17810 |
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systemic AL amyloidosis
|
17816 |
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localized AL amyloidosis
|
17817 |
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primary localized amyloidosis
|
17817 |
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autosomal dominant beta2-microglobulinic amyloidosis
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17810 |
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lymphoma of bone
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17814 |
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lymphoma of bone tissue
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17814 |
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atypical dentin dysplasia due to SMOC2 deficiency
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17819 |
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severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion
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17811 |
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uterine corpus localized epithelial mesothelioma
|
1781 |
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bone tissue lymphoma
|
17814 |
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