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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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dentinogenesis imperfecta, shields type II
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D003811 |
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ovarian Seromucinous tumor
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3811 |
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ovarian seromucinous tumor
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3811 |
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mixed epithelial tumor of ovary
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3811 |
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mixed epithelial tumor of the ovary
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3811 |
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hernandez aguirre-negrete syndrome
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C538112 |
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hernández aguirre-negrete syndrome
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C538112 |
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asymmetry in the pigmentation of the irides
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C538115 |
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hersh podruch weisskopk syndrome
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C538114 |
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combined oxidative phosphorylation defect type 9
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13811 |
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combined oxidative phosphorylation deficiency 9
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13811 |
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combined oxidative phosphorylation deficiency 9; COXPD9
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http://purl.obolibrary.org/obo/MONDO_0013811 |
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combined oxidative phosphorylation deficiency caused by mutation in MRPL3
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13811 |
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combined oxidative phosphorylation deficiency type 9
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13811 |
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ehlers-danlos syndrome with progeroid facies and mild mental retardation
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C538112 |
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