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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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steroid-sensitive nephrotic syndrome
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44781 |
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pignata guarino syndrome
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C536781 |
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partial 6q+ syndrome
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C537810 |
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7p2 monosomy syndrome
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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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trisomy 6q syndrome, partial
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C537810 |
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central nervous system toxoplasmosis
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D016781 |
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chromosome 7, terminal 7p deletion (del 7p21-p22)
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C537818 |
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lymphoma of the bone
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17814 |
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orofaciodigital syndrome, thurston type
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C557819 |
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atopy, susceptibility to
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7817 |
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chromosome 6, trisomy 6p
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C537811 |
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chromosome 6, trisomy 6q
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C537812 |
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chromosome 6, trisomy 6q2
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C537810 |
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