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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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disease, deficiency
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D003677 |
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diseases, deficiency
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D003677 |
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duplication xq13 1 q21 1
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C536753 |
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childhood glaucoma (disease)
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20367 |
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pediatric glaucoma (disease)
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20367 |
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gastric leiomyosarcoma (disease)
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3367 |
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trisomy xq13 1 q21 1
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C536753 |
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duplication xq13 1 q21 1 x chromosome
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C536753 |
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complementation group 1 xeroderma pigmentosum
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C536765 |
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T-cell lymphoma 1a
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C536782 |
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myocardial infarction (disease) of cardiac septum
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3671 |
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myocardial infarction (disease) of subendocardium layer
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3674 |
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syphilitic myelopathy (tabes dorsalis)
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C536776 |
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Heart-hand syndrome 2
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C536784 |
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transient neonatal, 2 diabetes mellitus
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C563672 |
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