Name | Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type |
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Synonym | Phosphodiester Glycoside Deficiency |
Categories | Genetic disease (inborn) | Metabolic disease |
MeSH® ID | C563601 |
1. |
Diseases
←
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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2. |
Diseases
←
Nutritional and Metabolic Diseases
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