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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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familial, 1 hypobetalipoproteinemia
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C566267 |
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congenital, with spastic ataxia miosis
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C566247 |
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B coli infection
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5662 |
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Balantidium coli infection
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5662 |
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bilateral atresia of, with congenital vertical talus external auditory canal
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C566245 |
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amorph type rh-null disease
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C566210 |
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internal anal sphincter myopathy
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C566287 |
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alpha-1 protease inhibitor deficiency
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C566273 |
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icelandic type peripapillary chorioretinal degeneration
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C566236 |
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fibrosing syndrome, peritoneal
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D056627 |
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fibrosing syndromes, peritoneal
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D056627 |
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scleroses, encapsulating peritoneal
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D056627 |
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sclerosis, encapsulating peritoneal
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D056627 |
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infusion site reaction
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D000075662 |
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injection site reaction
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D000075662 |
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