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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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ornithine aminotransferase deficiency
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9796 |
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ornithine ketoacid aminotransferase deficiency
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9796 |
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Fuchs gyrate atrophy of the choroid and retina
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9796 |
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Fuchs gyrate atrophy
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9796 |
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hyperornithinemia with gyrate atrophy of choroid and retina
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9796 |
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gyrate atrophy of choroid and retina
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9796 |
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hyperornithinemia-gyrate atrophy of choroid and retina syndrome
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9796 |
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gyrate atrophy of choroid and retina; GACR
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http://purl.obolibrary.org/obo/MONDO_0009796 |
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Girate atrophy of the retina
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9796 |
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gyrate atrophy of the retina
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9796 |
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gyrate atrophy of the choroid and/or retina
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9796 |
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