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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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variant ABeta2M amyloidosis
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17810 |
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systemic AL amyloidosis
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17816 |
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localized AL amyloidosis
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17817 |
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primary localized amyloidosis
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17817 |
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spinocerebellar ataxia 17
|
11781 |
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spinocerebellar ataxia 17; SCA17
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http://purl.obolibrary.org/obo/MONDO_0011781 |
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Huntington disease-like 4
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11781 |
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systemic Immunoglobulin Light chain amyloidosis
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17816 |
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uterine corpus adenomatoid tumor
|
1781 |
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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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uterine corpus localized epithelial mesothelioma
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1781 |
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severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion
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17811 |
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bone tissue lymphoma
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17814 |
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