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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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malignant neoplasm of the carotid body
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4650 |
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malignant tumor of the carotid body
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4650 |
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age at onset of parkinson disease
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C564653 |
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progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RNASEH1
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14656 |
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progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2
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14656 |
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progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2; PEOB2
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http://purl.obolibrary.org/obo/MONDO_0014656 |
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progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 2
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14656 |
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progressive external ophthalmoplegia, autosomal recessive 2
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14656 |
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skull disease or disorder
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24654 |
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fibrous sarcoma of the synovium
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3465 |
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myelogenous, aggressive phase leukemia
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D015465 |
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oncocytic carcinoma of thyroid
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6465 |
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c12orf65-related combined oxidative phosphorylation defect
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44655 |
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carotid body paraganglioma, malignant
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4650 |
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x-linked spastic paraplegia 34
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C567465 |
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