5C61.5

ICD-11 MMS 2026-01

Disorders of facilitated glucose transport

Index terms

  • Disorders of facilitated glucose transport
  • Encephalopathy due to GLUT1 deficiency
  • Facilitated glucose transporter protein type 1 deficiency
Show allHide
  • Glucose transporter defect, blood-brain barrier
  • Familial renal glucosuria
  • SGLT2 deficiency

Exclusions from above levels

  • 3A10.Z – Hereditary haemolytic anaemia due to enzyme deficiency
  • 5A71.01 – Congenital adrenal hyperplasia
  • 5A81.1 – 5-alpha-reductase deficiency
Show allHide
  • 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

  • 5C61.0 – Glucose-galactose malabsorption
  • 5C61.1 – Maltase-glucoamylase deficiency
  • 5C61.2 – Congenital sucrase-isomaltase deficiency
  • 5C61.3 – Alpha, alpha trehalase deficiency
  • 5C61.4 – Acquired monosaccharide malabsorption
  • 5C61.6 – Lactose intolerance
  • 5C61.Y – Other specified disorders of carbohydrate absorption or transport
  • 5C61.Z – Disorders of carbohydrate absorption or transport, unspecified

Foundation entity

Disorders of facilitated glucose transport – http://id.who.int/icd/entity/1088155670

Part of: 5C61: Disorders of carbohydrate absorption or transport › 05: Endocrine, nutritional or metabolic diseases