5C56.20

ICD-11 MMS 2026-01

Mucolipidosis

Index terms

  • Mucolipidosis
  • Mucolipidosis type 3
  • Pseudo-Hurler disease
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  • Pseudo-Hurler polydystrophy
  • Mucolipidosis type 2
  • I-cell disease
  • Inclusion cell disease
  • N-acetyl-glucosamine 1-phosphotransferase deficiency

Excludes

  • 5C56.21 – Sialidosis (mucolipidosis type 1)

Exclusions from above levels

  • 5C51.3 – Glycogen storage disease due to LAMP-2 deficiency
  • http://id.who.int/icd/entity/1191191920 – Disorders of lipoprotein metabolism or certain specified lipidaemias
  • 3A10.Z – Hereditary haemolytic anaemia due to enzyme deficiency
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  • 5A71.01 – Congenital adrenal hyperplasia
  • 5A81.1 – 5-alpha-reductase deficiency
  • LD28.01 – Marfan syndrome
  • LD28.1 – Ehlers-Danlos syndrome
  • LD2A.4 – androgen resistance syndrome
  • 18 – Pregnancy, childbirth or the puerperium
  • http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn

Sibling codes

  • 5C56.21 – Oligosaccharidosis
  • 5C56.2Y – Other specified glycoproteinosis
  • 5C56.2Z – Glycoproteinosis, unspecified

Foundation entity

Mucolipidosis – http://id.who.int/icd/entity/714623911

Part of: 5C56.2: Glycoproteinosis › 5C56: Lysosomal diseases › 05: Endocrine, nutritional or metabolic diseases