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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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Noack syndrome
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C0220658 |
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PFEIFFER SYNDROME
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C0220658 |
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Pfeiffer Syndrome
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C0220658 |
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Pfeiffer syndrome
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C0220658 |
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Pfeiffer-type acrocephalosyndactyly
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C0220658 |
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Syndrome, Noack
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C0220658 |
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Syndrome, Pfeiffer
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C0220658 |
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Syndromes, Noack
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C0220658 |
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craniofacial-skeletal-Dermatologic dysplasia
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C0220658 |
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Acrocephalosyndactyly type 5
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C0220658 |
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Acrocephalosyndactyly, type 5
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C0220658 |
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acrocephalosyndactyly type 5
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C0220658 |
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acrocephalosyndactyly, type 5
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C0220658 |
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Type V Acrocephalosyndactylies
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C0220658 |
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Type V Acrocephalosyndactyly
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C0220658 |
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