KA8F

ICD-11 MMS 2026-01

Neonatal vitamin K deficiency

Description

There are 3 forms of vitamin K–deficiency bleeding (VKDB) of the newborn. Early VKDB (haemorrhagic disease of the newborn) that occurs at 1-14 days of age. The most common sites of bleeding are the gastrointestinal tract, mucosal and cutaneous tissue, the umbilical stump, and the post-circumcision site. Late VKDB most commonly occurs at 2-12 weeks of age, although cases can occur up to 6 months. The most common site of bleeding is intracranial, although cutaneous and gastrointestinal bleeding may be initial manifestation. The third form of VKDB occurs at birth or shortly thereafter. It is secondary to maternal intake of medications (warfarin, phenobarbital, phenytoin) that cross the placenta.

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.

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

Child codes

  • KA8F.0 – Diffuse bleeding diathesis due to vitamin K deficient haemorrhagic disease of fetus or newborn
  • KA8F.Y – Other specified neonatal vitamin K deficiency
  • KA8F.Z – Neonatal vitamin K deficiency, unspecified

Sibling codes

  • KA80 – Fetal blood loss
  • KA81 – Umbilical haemorrhage of newborn
  • KA82 – Intracranial nontraumatic haemorrhage of fetus or newborn
  • KA83 – Certain specified neonatal haemorrhages
  • KA84 – Haemolytic disease of fetus or newborn
  • KA85 – Hydrops fetalis due to haemolytic disease
  • KA86 – Neonatal kernicterus
  • KA87 – Neonatal hyperbilirubinaemia
  • KA88 – Disseminated intravascular coagulation of fetus or newborn
  • KA89 – Transient neonatal thrombocytopaenia
  • KA8A – Polycythaemia neonatorum
  • KA8B – Anaemia of prematurity
  • KA8C – Congenital hypoplastic anaemia
  • KA8D – Transient neonatal neutropaenia
  • KA8E – Alloimmune neonatal neutropaenia
  • KA8Y – Other specified haemorrhagic or haematological disorders of fetus or newborn
  • KA8Z – Haemorrhagic or haematological disorders of fetus or newborn, unspecified

Foundation entity

Neonatal vitamin K deficiency – http://id.who.int/icd/entity/3517042

Part of: 19: Certain conditions originating in the perinatal period