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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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carnitine deficiency, systemic primary
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C536778 |
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carnitine deficiency, systemic, due to defect in renal reabsorption of carnitine
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C536778 |
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zori stalker williams syndrome
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C536728 |
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chromosome xq trisomy
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C536732 |
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chromosome 22, trisomy
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C536799 |
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chromosome 2, trisomy 2q
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C535367 |
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chromosome 22 trisomy mosaic
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C536796 |
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x chromosome, trisomy xp3
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C536756 |
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x chromosome, trisomy xpter xq13
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C536731 |
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x chromosome, trisomy xq
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C536732 |
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x chromosome, trisomy xq25
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C536733 |
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xeroderma pigmentosum, type 9
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C536765 |
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wolffian adnexal tumor
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C536741 |
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female adnexal tumor of probable wolffian origin
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C536741 |
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micrognathia, absent thumbs, & distal aphalangia cleidocranial dysplasia
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C536719 |
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