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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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ACHM2
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C1857618 |
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RMCH2
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C1857618 |
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ACHROMATOPSIA 2
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C1857618 |
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Achromatopsia 2
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C1857618 |
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CNGA3 achromatopsia
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C1857618 |
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COLORBLINDNESS, TOTAL
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C1857618 |
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Colorblindness, Total
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C1857618 |
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Colorblindness, total
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C1857618 |
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Total colorblindness
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C1857618 |
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achromatopsia 2
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C1857618 |
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colorblindness, total
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C1857618 |
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achromatopsia caused by mutation in CNGA3
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C1857618 |
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ROD MONOCHROMACY 2
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C1857618 |
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ROD MONOCHROMATISM 2
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C1857618 |
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Rod monochromacy 2
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C1857618 |
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