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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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autosomal dominant hyperimmunoglobulin E syndrome
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7818 |
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terminal 7p deletion (del 7p21-p22) chromosome 7
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C537818 |
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insulin-dependent, 24 diabetes mellitus
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C567818 |
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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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chromosome 7, monosomy 7p2
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C537818 |
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type IX oral facial digital syndrome
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C557818 |
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partial deletion of short arm (7p2-) chromosome 7
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C537818 |
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type 9 orofaciodigital syndrome
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C557818 |
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chromosome 7, terminal 7p deletion (del 7p21-p22)
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C537818 |
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chromosome 7, partial deletion of short arm (7p2-)
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C537818 |
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chromosome 7, partial monosomy 7p
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C537818 |
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lethal arteriopathy syndrome due to fibulin-4 deficiency
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17818 |
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hyperimmunoglobulin E syndrome type 1
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7818 |
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hyperimmunoglobulin E recurrent infection syndrome, autosomal dominant
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7818 |
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