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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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brancher deficiency glycogenosis
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C0017923 |
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branching-transferase deficiency glycogenosis
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C0017923 |
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GSD IV, neuromuscular form, childhood
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C0017923 |
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GSD IV, neuromuscular form, congenital
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C0017923 |
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GSD IV, neuromuscular form, fatal perinatal
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C0017923 |
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GBE1 glycogen storage disease
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C0017923 |
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GSD IV, nonprogressive hepatic
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C0017923 |
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GSD due to glycogen branching enzyme deficiency
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C0017923 |
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Glycogenosis due to glycogen branching enzyme deficiency
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C0017923 |
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glycogenosis due to glycogen branching enzyme deficiency
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C0017923 |
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Cirrhosis, familial, with deposition of abnormal glycogen
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C0017923 |
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cirrhosis, familial, with deposition of abnormal glycogen
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C0017923 |
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