LA05.0 Microcephaly
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01
A condition caused by failure of the head to correctly develop during the antenatal period. This condition is characterised by a head size that is significantly smaller than normal for their age and sex. This condition may also present with developmental delays, difficulties with balance and coordination, short stature, hyperactivity, mental retardation, seizures, or other neurological abnormalities.
inclusions
- Micrencephaly
exclusions
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
synonyms
- Microcephaly
- Micrencephalon
- Micrencephaly
- Microencephaly
- brain hypoplasia
- brain nondevelopment
- cephalic hypoplasia
- congenital microcephaly
- microcephalic
- microcephalus
- nanocephaly
- undeveloped brain
- undeveloped cerebrum
- Congenital skull deformity with microcephaly
- absence of skull bone with microcephaly
- anomaly of skull with microcephaly
- skull agenesis with microcephaly
- Hydromicrocephaly
- Autosomal dominant primary microcephaly
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