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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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AIFBL
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C4225218 |
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AIFBL1
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C4225218 |
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Hereditary pediatric Behçet-like disease
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C4225218 |
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hereditary paediatric Behçet-like disease
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C4225218 |
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hereditary pediatric Behçet-like disease
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C4225218 |
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Behçet-like disease due to HA20
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C4225218 |
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AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE 1
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C4225218 |
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Autoinflammatory syndrome, familial, Behcet-like 1
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C4225218 |
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autoinflammatory syndrome, familial, Behcet-like 1
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C4225218 |
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Behçet-like disease due to haploinsufficiency of A20
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C4225218 |
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