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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.
mental retardation, X-linked, syndromic type 10
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C3266731 |
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HSD10 mitochondrial disease, X-linked dominant
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C3266731 |
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chorioathetosis with mental retardation and abnormal behavior
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C3266731 |
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chorioathetosis with mental retardation and abnormal behaviour
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C3266731 |
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mental retardation with chorioathetosis and abnormal behavior
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C3266731 |
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mental retardation with chorioathetosis and abnormal behaviour
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C3266731 |
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