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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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genetic essential hypertension
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7781 |
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severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion
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17811 |
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dominant congenital ichthyosiform erythroderma
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7810 |
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bullous type ichthyosis
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7813 |
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superficial epidermolytic ichthyosis
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7813 |
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autosomal dominant ichthyosis vulgaris
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7810 |
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type I immediate hypersensitivity reaction
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7817 |
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acute myocardial infarction
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4781 |
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acute myocardial infarction (disease)
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4781 |
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hyperimmunoglobulin E-recurrent infection syndrome
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7818 |
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Hyper-IgE recurrent infection syndrome 1
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7818 |
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hyper-IgE recurrent infection syndrome, autosomal dominant
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7818 |
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deficiency of interleukin 1 receptor antagonist
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C557815 |
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deficiency of interleukin(IL)-1 receptor antagonist
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C557815 |
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deficiency of interleukin-1 receptor antagonist (DIRA)
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C557815 |
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