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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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ALGS1
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C1956125 |
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Alagille-Watson syndrome
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C1956125 |
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arteriohepatic dysplasia
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C1956125 |
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ALAGILLE SYNDROME 1
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C1956125 |
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Alagille Syndrome 1
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C1956125 |
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Alagille syndrome 1
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C1956125 |
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HEPATIC DUCTULAR HYPOPLASIA, SYNDROMATIC
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C1956125 |
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JAG1-Related Alagille Syndrome
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C1956125 |
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Syndromic bile duct paucity due to a JAG1 point mutation
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C1956125 |
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syndromic bile duct paucity due to a JAG1 point mutation
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C1956125 |
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Alagille syndrome due to a JAG1 point mutation
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C1956125 |
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Alagille-Watson syndrome due to a JAG1 point mutation
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C1956125 |
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Arteriohepatic dysplasia due to a JAG1 point mutation
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C1956125 |
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arteriohepatic dysplasia due to a JAG1 point mutation
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C1956125 |
|
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hepatic ductular hypoplasia, syndromatic
|
C1956125 |
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