5C56.21 Oligosaccharidosis

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

synonyms

• Oligosaccharidosis
• Aspartylglucosaminuria
• Aspartylglucosaminidase deficiency
• Alpha-mannosidosis
• Lysosomal alpha-D-mannosidase deficiency
• Infantile alpha-mannosidosis
• Adult alpha-mannosidosis
• Beta-mannosidosis
• Lysosomal beta-mannosidase deficiency
• Mannosidosis, not otherwise specified
• mannosidase deficiency
• Fucosidosis
• Alpha-L-fucosidase deficiency
• Sialidosis
• Mucolipidosis type 1
• Sialidosis type 1
• Cherry-red-spot-myoclonus syndrome
• Lipomucopolysaccharidosis
• Normomorphic sialidosis
• Sialidosis type 2
• Infantile dysmorphic sialidosis
• Congenital sialidosis type 2
• Juvenile sialidosis type 2
• Alpha-N-acetylgalactosaminidase deficiency
• N-acetyl-alpha-D-galactosaminidase deficiency
• NAGA - [Alpha-N-acetylgalactosaminidase] deficiency
• Alpha-N-acetylgalactosaminidase deficiency type 1
• Schindler disease type 1
• Schindler disease
• NAGA deficiency type 1 - [Alpha-N-acetylgalactosaminidase deficiency type 1]
• Alpha-N-acetylgalactosaminidase deficiency type 2
• Adult-onset Alpha-N-acetylgalactosaminidase deficiency
• Schindler disease type 2
• Kanzaki disease
• NAGA deficiency type 2 - [Alpha-N-acetylgalactosaminidase deficiency type 2]
• Alpha-N-acetylgalactosaminidase deficiency type 3
• Schindler disease type 3
• NAGA deficiency type 3 - [Alpha-N-acetylgalactosaminidase deficiency type 3]
• Galactosialidosis
• Neuraminidase deficiency with beta-galactosidase deficiency
• Goldberg syndrome
• Combined deficiency of neuraminidase and beta-galactosidase
• Protective protein deficiency

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