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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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rod monochromacy 1, formerly
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C1849792 |
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rod monochromatism 1, formerly
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C1849792 |
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achromatopsia type 3
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C1849792 |
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ACHROMATOPSIA WITH MYOPIA
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C1849792 |
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Total colorblindness with myopia
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C1849792 |
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achromatopsia caused by mutation in CNGB3
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C1849792 |
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Achromatopsia with myopia
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C1849792 |
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achromatopsia with myopia
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C1849792 |
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total colorblindness with myopia
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C1849792 |
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