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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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systemic Immunoglobulin Light chain amyloidosis
|
17816 |
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Sidransky Feinstein Goodman syndrome
|
7811 |
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autosomal dominant HIES
|
7818 |
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variant ABeta2M amyloidosis
|
17810 |
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ichthyosis hystrix Rheydt type
|
18781 |
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Van Maldergem Wetzburger Verloes syndrome
|
17813 |
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uterine corpus adenomatoid tumor
|
1781 |
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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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oligodactylous clubfeet, and anonychia-nail hypoplasia syndrome fibular agenesis-hypoplasia
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C567819 |
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acute bronchitis and bronchiolitis
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3781 |
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congenital alopecia and nail dystrophy T-cell immunodeficiency
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C536781 |
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congenital alopecia, and nail dystrophy t-cell immunodeficiency
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C536781 |
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keratitis, ichthyosis, and deafness (KID) syndrome
|
18781 |
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