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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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COXPD7
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13306 |
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combined oxidative phosphorylation defect type 7
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13306 |
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combined oxidative phosphorylation deficiency 7
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13306 |
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combined oxidative phosphorylation deficiency 7; COXPD7
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http://purl.obolibrary.org/obo/MONDO_0013306 |
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combined oxidative phosphorylation deficiency caused by mutation in C12ORF65
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13306 |
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combined oxidative phosphorylation deficiency caused by mutation in C12orf65
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13306 |
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combined oxidative phosphorylation deficiency type 7
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13306 |
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severe C12ORF65-related COXPD
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13306 |
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severe C12ORF65-related combined oxidative phosphorylation defect
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13306 |
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C12ORF65 combined oxidative phosphorylation deficiency
|
13306 |
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C12orf65 combined oxidative phosphorylation deficiency
|
13306 |
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