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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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ASGD3
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C1866560 |
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IGDA
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C1866560 |
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IRID1
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C1866560 |
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IRIDOGONIODYSGENESIS, TYPE 1
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C1866560 |
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FOXC1 iridogoniodysgenesis
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C1866560 |
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IGDA syndrome
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C1866560 |
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Iridogoniodysgenesis type1
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C1866560 |
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glaucoma iridogoniodysgenesia
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C1866560 |
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Iridogoniodysgenesis, Type 1
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C1866560 |
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iridogoniodysgenesis type 1
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C1866560 |
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iridogoniodysgenesis, type 1
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C1866560 |
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IRIDOGONIODYSGENESIS ANOMALY, AUTOSOMAL DOMINANT
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C1866560 |
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Anterior segment dysgenesis 3
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C1866560 |
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Iridogoniodysgenesis anomaly, Autosomal dominant
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C1866560 |
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iridogoniodysgenesis caused by mutation in FOXC1
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C1866560 |
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