3A72.00

ICD-11 MMS 2026-01

Hereditary sideroblastic anaemias

Index terms

  • Hereditary sideroblastic anaemias
  • Autosomal recessive sideroblastic anaemia
  • Sex-linked hypochromic sideroblastic anaemia
Show allHide
  • familial sex linked hypochromic anaemia
  • X-linked sideroblastic anaemia, pyridoxine-responsive
  • Erythroid 5-aminolevulinate synthase deficiency
  • Autosomal dominant sideroblastic anaemia
  • Autosomal recessive congenital sideroblastic anaemia
  • Severe congenital hypochromic anaemia with ringed sideroblasts
  • Autosomal recessive sideroblastic anaemia, pyridoxine-refractory
  • Adult-onset autosomal recessive sideroblastic anaemia

Inclusions

  • Sex-linked hypochromic sideroblastic anaemia
  • X-linked sideroblastic anaemia, pyridoxine-responsive
  • Autosomal recessive sideroblastic anaemia, pyridoxine-refractory

Exclusions from above levels

  • 04 – Diseases of the immune system
  • 05 – Endocrine, nutritional or metabolic diseases
  • 18 – Complications of pregnancy, childbirth or the puerperium
Show allHide
  • 19 – Certain conditions originating in the perinatal period
  • 20 – Congenital malformations, deformations or chromosomal abnormalities
  • 22 – Injury, poisoning or certain other consequences of external causes
  • http://id.who.int/icd/entity/1000704511 – Human immunodeficiency virus disease
  • JB64.1 – Other diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism complicating pregnancy, childbirth or the puerperium

Sibling codes

  • 3A72.01 – Hereditary syndromic sideroblastic anaemia
  • 3A72.0Y – Other specified congenital sideroblastic anaemias
  • 3A72.0Z – Congenital sideroblastic anaemias, unspecified

Foundation entity

Hereditary sideroblastic anaemias – http://id.who.int/icd/entity/853645278

Part of: 3A72.0: Congenital sideroblastic anaemias › 3A72: Sideroblastic anaemia › 03: Diseases of the blood or blood-forming organs