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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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congenital betalipoprotein deficiency syndrome
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C0000744 |
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Microsomal Triglyceride Transfer Protein Deficiency
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C0000744 |
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Microsomal Triglyceride Transfer Protein Deficiency Disease
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C0000744 |
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apolipoprotein B deficiency
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C0000744 |
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Homozygous familial hypobetalipoproteinemia
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C0000744 |
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Betalipoprotein deficiency disease
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C0000744 |
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homozygous familial hypobetalipoproteinemia
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C0000744 |
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Low-density beta lipoprotein deficiency
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C0000744 |
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Microsomal-triglyceride transfer protein deficiency
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C0000744 |
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Bassen Kornzweig syndrome
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C0000744 |
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microsomal triglyceride transfer Protein deficiency
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C0000744 |
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Microsomal triglyceride transfer protein deficiency disease
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C0000744 |
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microsomal triglyceride transfer protein deficiency disease
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C0000744 |
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