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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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3-Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency
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C3266731 |
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Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency
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C3266731 |
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MENTAL RETARDATION WITH CHOREOATHETOSIS AND ABNORMAL BEHAVIOR
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C3266731 |
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17-BETA-HYDROXYSTEROID DEHYDROGENASE X DEFICIENCY
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C3266731 |
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mental retardation, X-linked syndromic 10
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C3266731 |
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mental retardation, X-linked, syndromic 10
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C3266731 |
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mental retardation, X-linked, syndromic type 10
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C3266731 |
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17-Beta-Hydroxysteroid Dehydrogenase X Deficiency
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C3266731 |
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17-beta-hydroxysteroid dehydrogenase X deficiency
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C3266731 |
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MENTAL RETARDATION, X-LINKED, SYNDROMIC 10
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C3266731 |
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Mental Retardation, X-Linked, Syndromic 10
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C3266731 |
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HSD10 mitochondrial disease
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C3266731 |
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2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency
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C3266731 |
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2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency
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C3266731 |
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3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency
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C3266731 |
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