5C56.21
Oligosaccharidosis
Oligossacaridose
CategoryIndex Terms
OligosaccharidosisAspartylglucosaminuriaAspartylglucosaminidase deficiencyAlpha-mannosidosisLysosomal alpha-D-mannosidase deficiencyInfantile alpha-mannosidosisAdult alpha-mannosidosisBeta-mannosidosisLysosomal beta-mannosidase deficiencyMannosidosis, not otherwise specifiedmannosidase deficiencyFucosidosisAlpha-L-fucosidase deficiencySialidosisMucolipidosis type 1Sialidosis type 1Cherry-red-spot-myoclonus syndromeLipomucopolysaccharidosisNormomorphic sialidosisSialidosis type 2Infantile dysmorphic sialidosisCongenital sialidosis type 2Juvenile sialidosis type 2Alpha-N-acetylgalactosaminidase deficiencyN-acetyl-alpha-D-galactosaminidase deficiencyNAGA - [Alpha-N-acetylgalactosaminidase] deficiencyAlpha-N-acetylgalactosaminidase deficiency type 1Schindler disease type 1Schindler diseaseNAGA deficiency type 1 - [Alpha-N-acetylgalactosaminidase deficiency type 1]Alpha-N-acetylgalactosaminidase deficiency type 2Adult-onset Alpha-N-acetylgalactosaminidase deficiencySchindler disease type 2Kanzaki diseaseNAGA deficiency type 2 - [Alpha-N-acetylgalactosaminidase deficiency type 2]Alpha-N-acetylgalactosaminidase deficiency type 3Schindler disease type 3NAGA deficiency type 3 - [Alpha-N-acetylgalactosaminidase deficiency type 3]GalactosialidosisNeuraminidase deficiency with beta-galactosidase deficiencyGoldberg syndromeCombined deficiency of neuraminidase and beta-galactosidaseProtective protein deficiency