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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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ALGS2
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C1857761 |
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Syndromic bile duct paucity due to a NOTCH2 point mutation
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C1857761 |
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syndromic bile duct paucity due to a NOTCH2 point mutation
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C1857761 |
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Alagille syndrome due to a NOTCH2 point mutation
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C1857761 |
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Alagille-Watson syndrome due to a NOTCH2 point mutation
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C1857761 |
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Arteriohepatic dysplasia due to a NOTCH2 point mutation
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C1857761 |
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ALAGILLE SYNDROME 2
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C1857761 |
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Alagille Syndrome 2
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C1857761 |
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Alagille syndrome 2
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C1857761 |
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Alagille syndrome type 2
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C1857761 |
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