KA8F.0

ICD-11 MMS 2026-01

Diffuse bleeding diathesis due to vitamin K deficient haemorrhagic disease of fetus or newborn

Description

Haemorrhagic disease of the newborn is a bleeding disorder of the newborn usually seen in the first week after life when vitamin K replacement is not provided to the newborn infant immediately after birth and is primarily characterised by gastrointestinal bleeding. The disorder can also be seen later in the newborn period in breast fed infants of vitamin K deficient mothers.

Coding note from above levels

Conditions arising in the perinatal period, even though death or morbidity occurs later, should, as far as possible, be coded to chapter 19, which takes precedence over chapters containing codes for diseases by their anatomical site. For children less than 28 days old, assume that a reported condition developed in the perinatal period, unless the duration is stated and the onset was after the first completed week of life.

Index terms

  • Diffuse bleeding diathesis due to vitamin K deficient haemorrhagic disease of fetus or newborn
  • Diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of fetus and newborn
  • newborn haemorrhagic disorder
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  • newborn vitamin K deficiency
  • Diffuse bleeding diathesis due to vitamin K deficient haemorrhagic disease of fetus or newborn, early
  • Diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of fetus and newborn, early
  • Diffuse bleeding diathesis due to vitamin K deficient haemorrhagic disease of fetus or newborn, classic
  • Diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of fetus and newborn, classic
  • Diffuse bleeding diathesis due to vitamin K deficient haemorrhagic disease of fetus or newborn, late
  • Diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of fetus and newborn, late

Exclusions from above levels

  • 3A10 – Hereditary haemolytic anaemia
  • 5C58.00 – Crigler-Najjar syndrome
  • 5C58.01 – Gilbert syndrome
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  • 5C58.02 – Dubin-Johnson syndrome
  • LB20.22 – Congenital stenosis or stricture of bile ducts
  • 01 – Certain infectious or parasitic diseases - acquired after birth
  • 02 – Neoplasms
  • 05 – Endocrine, nutritional or metabolic diseases
  • 08 – Certain congenital diseases of the nervous system
  • 20 – Congenital malformations, deformations and chromosomal abnormalities
  • 22 – Injury, poisoning or certain other consequences of external causes
  • 4A01.03 – Transient hypogammaglobulinaemia of infancy
  • 9B71.3 – Retinopathy of prematurity
  • BC43 – congenital cardiomyopathy
  • DA93.0 – Paralytic ileus
  • EA50.Z – Pemphigus neonatorum
  • EH40.00 – Cradle cap
  • http://id.who.int/icd/entity/588616678 – Gastroenteritis or colitis of infectious origin
  • http://id.who.int/icd/entity/609214049 – Congenital gonococcal infection

Sibling codes

  • KA8F.Y – Other specified neonatal vitamin K deficiency
  • KA8F.Z – Neonatal vitamin K deficiency, unspecified

Foundation entity

Diffuse bleeding diathesis due to vitamin K deficient haemorrhagic disease of fetus or newborn – http://id.who.int/icd/entity/1599946610

Part of: KA8F: Neonatal vitamin K deficiency › 19: Certain conditions originating in the perinatal period