KB61.2ICD-11 MMS 2026-01
Neonatal hypocalcaemia
Description
Hypocalcaemia is a common metabolic problem in newborns. In the neonate, hypocalcaemia is defined by birth weight (BW) categories. In infants with BW greater than 1500 g, hypocalcaemia is defined as a total serum calcium (Ca) concentration less than 8 mg/dL (2 mmol/L) or an ionized fraction of less than 4.4 mg/dL (1.1 mmol/L). In very low birth weight premature infants (BW<1500 g), hypocalcaemia is defined as a total serum Ca concentration less than 7 mg/dL (1.75 mmol/L) or an ionized fraction of less than 4 mg/dL (1 mmol/L). Aetiologies of early hypocalcaemia (occurs in the first two to three days after birth) include prematurity, maternal diabetes, birth asphyxia, and intrauterine growth. Causes of late hypocalcaemia (usually occurs at the end of the first week of life) include hypoparathyroidism and high phosphate intake. Most infants with hypocalcaemia are asymptomatic. If symptomatic, neuromuscular irritability is the most common sign with jitteriness and muscle jerking. Less common findings include seizures, and rarely laryngospasm, wheezing, or vomiting.
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
- Neonatal hypocalcaemia
- Cow milk hypocalcaemia in newborn
- cow's milk hypocalcaemia in newborn
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- Phosphate-loading hypocalcaemia
Excludes
KB64– Transitory neonatal hypoparathyroidism
Exclusions from above levels
01– Certain infectious or parasitic diseases - acquired after birth02– Neoplasms05– Endocrine, nutritional or metabolic diseases
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08– Certain congenital diseases of the nervous system20– Congenital malformations, deformations and chromosomal abnormalities22– Injury, poisoning or certain other consequences of external causes3A10– Hereditary haemolytic anaemia4A01.03– Transient hypogammaglobulinaemia of infancy9B71.3– Retinopathy of prematurityBC43– congenital cardiomyopathyDA93.0– Paralytic ileusEA50.Z– Pemphigus neonatorumEH40.00– 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
KB61.0– Neonatal hypomagnesaemiaKB61.1– Neonatal tetany without calcium or magnesium deficiencyKB61.3– Neonatal osteopeniaKB61.Y– Other specified transitory neonatal disorders of calcium or magnesium metabolismKB61.Z– Transitory neonatal disorders of calcium or magnesium metabolism, unspecified
Foundation entity
Neonatal hypocalcaemia – http://id.who.int/icd/entity/549613748
Part of: KB61: Transitory neonatal disorders of calcium or magnesium metabolism › 19: Certain conditions originating in the perinatal period