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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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blepharophimosis and mental retardation syndrome, say-barber-biesecker-young-simpson type
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C536717 |
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chromosome 22, microdeletion 22 q11
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C536797 |
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fatal multiple mitochondrial dysfunctions syndrome caused by mutation in BOLA3
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13675 |
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complete hydatidiform mole caused by mutation in KHDC3L
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13671 |
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x chromosome, monosomy xp22 pter
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C536754 |
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x chromosome, monosomy xq28
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C536755 |
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trisomy 22 mosaic
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C536796 |
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trisomy 22 mosaicism syndrome
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C536796 |
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variant form mucolipidosis III
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C565367 |
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BOLA3 fatal multiple mitochondrial dysfunctions syndrome
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13675 |
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true posterior myocardial infarction
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3672 |
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cardiac septum myocardial infarction (disease)
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3671 |
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subendocardium layer myocardial infarction (disease)
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3674 |
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malignant kidney neoplasm
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2367 |
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malignant renal neoplasm
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2367 |
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