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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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AEL
|
17858 |
|
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AML-M6
|
17858 |
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Erythroleukemia
|
17858 |
|
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Kppp1
|
7858 |
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PPKP1A
|
7858 |
|
|
AML M6
|
17858 |
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|
FAB M6
|
17858 |
|
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acute erythroleukemia
|
17858 |
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erythroblastic leukemia
|
17858 |
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punctate palmoplantar keratoderma caused by mutation in AAGAB
|
7858 |
|
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foveal hypoplasia and presenile cataract syndrome
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C537858 |
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presenile cataract foveal hypoplasia
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C537858 |
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acute erythroleukemia M6a subtype
|
17858 |
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acute erythroleukemia M6b subtype
|
17858 |
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inherited fatty acid metabolism disorder
|
37858 |
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