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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 2 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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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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3-Hydroxy-2-Methylbutyryl-CoA Dehydrogenase Deficiency
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C3266731 |
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3-HYDROXYACYL-CoA DEHYDROGENASE II DEFICIENCY
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C3266731 |
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3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
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C3266731 |
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Hydroxyacyl-CoA Dehydrogenase II Deficiency
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C3266731 |
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Hydroxyacyl-CoA dehydrogenase II deficiency
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C3266731 |
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hydroxyacyl-CoA dehydrogenase II deficiency
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C3266731 |
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CHOREOATHETOSIS WITH MENTAL RETARDATION AND ABNORMAL BEHAVIOR
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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 Behavior
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C3266731 |
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17beta-Hydroxysteroid Dehydrogenase Type 10 Deficiency
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C3266731 |
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3-Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency
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C3266731 |
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