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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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Meier-Gorlin syndrome caused by mutation in ORC4
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13428 |
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retinitis pigmentosa caused by mutation in PDE6B
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13429 |
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retinitis pigmentosa caused by mutation in RPE65
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13425 |
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type II complement component 8 deficiency
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13421 |
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type I complement component 8 deficiency
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13422 |
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type i complement component 8 deficiency
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http://purl.obolibrary.org/obo/MONDO_0013422 |
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C8B classic complement early component deficiency
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13421 |
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C8A classic complement early component deficiency
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13422 |
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C8 Beta deficiency
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13421 |
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C8 Alpha-gamma deficiency
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13422 |
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age-related macular degeneration caused by mutation in CX3CR1
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13420 |
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chromosome 3p deletion
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13424 |
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distal 3p deletion
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13424 |
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chromosome 3pter-p25 deletion syndrome
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13424 |
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nervous system diseases, parasympathetic
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D001342 |
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