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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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AMC1
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C4479539 |
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AMCNMY
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C4479539 |
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ARTHROGRYPOSIS MULTIPLEX CONGENITA 1, NEUROGENIC, WITH MYELIN DEFECT
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C4479539 |
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ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT
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C4479539 |
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Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect
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C4479539 |
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arthrogryposis multiplex congenita 1, neurogenic, with myelin defect
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C4479539 |
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Arthrogryposis multiplex congenita, neurogenic, with myelin defect
|
C4479539 |
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arthrogryposis multiplex congenita, neurogenic, with myelin defect
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C4479539 |
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