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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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classic complement early component deficiency caused by mutation in C8A
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13422 |
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classic complement early component deficiency caused by mutation in C8B
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13421 |
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carbohydrate deficient glycoprotein syndrome type IIf
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11342 |
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CX3CR1 age-related macular degeneration
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13420 |
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age related macular degeneration 12
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13420 |
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age related macular degeneration type 12
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13420 |
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congenital disorder of glycosylation type 2f
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11342 |
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chromosome 3, monosomy 3p25
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13424 |
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autonomic peripheral nervous system diseases
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D001342 |
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peripheral autonomic nervous system diseases
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D001342 |
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congenital disorder of glycosylation type IIf
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11342 |
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congenital disorder of glycosylation, type IIf
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11342 |
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congenital disorder of glycosylation, type IIf; CDG2F
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http://purl.obolibrary.org/obo/MONDO_0011342 |
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aneurysm - osteoarthritis syndrome
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13426 |
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chromosome 3p- syndrome
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13424 |
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