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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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fatal infantile, due to cytochrome c oxidase deficiency cardioencephalomyopathy
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C565784 |
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OXPHOS disease due to nDNA anomalies
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16578 |
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OXPHOS disease due to nuclear DNA anomalies
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16578 |
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fatal infantile, with cardioencephalomyopathy cytochrome c oxidase deficiency
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C565784 |
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mitochondrial oxidative phosphorylation disorder due to nDNA anomalies
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16578 |
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mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies
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16578 |
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advanced sleep-phase syndrome, familial
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C565789 |
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partial, with variable foci epilepsy
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C565785 |
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