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| language |
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| license |
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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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COXPD29
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14781 |
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COXPD36
|
54781 |
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myocardial infarction (disease), acute
|
4781 |
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acute myocardial infarction
|
4781 |
|
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acute myocardial infarction (disease)
|
4781 |
|
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combined oxidative phosphorylation deficiency 29
|
14781 |
|
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combined oxidative phosphorylation deficiency 29; COXPD29
|
14781 |
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combined oxidative phosphorylation deficiency 36
|
54781 |
|
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combined oxidative phosphorylation deficiency 36; COXPD36
|
http://purl.obolibrary.org/obo/MONDO_0054781 |
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combined oxidative phosphorylation deficiency caused by mutation in TXN2
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14781 |
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combined oxidative phosphorylation deficiency type 29
|
14781 |
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nephrotic syndrome of childhood - steroid sensitive
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44781 |
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steroid-responsive nephrotic syndrome
|
44781 |
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steroid-sensitive nephrotic syndrome
|
44781 |
|
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TXN2 combined oxidative phosphorylation deficiency
|
14781 |
|
