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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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cap disease
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C579969 |
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deficiency, ornithine aminotransferase
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D015799 |
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atrophy, gyrate
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D015799 |
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deficiency, OAT
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D015799 |
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deficiency, OKT
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D015799 |
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deficiency, ornithine-delta-aminotransferase
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D015799 |
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ornithine-delta-aminotransferase deficiency
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D015799 |
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ornithine keto acid aminotransferase deficiency
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D015799 |
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ornithine delta aminotransferase deficiency
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D015799 |
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ectodermal dysplasia, and cleft lip-palate syndrome 3 ectrodactyly
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C565799 |
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mitochondrial recessive ataxia syndrome
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C579922 |
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hookworm infectious disease
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5799 |
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Chmp2b-Related frontotemporal dementia
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C579991 |
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familial nonspecific dementia
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C579991 |
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ornithinemia with gyrate atrophy
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D015799 |
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