LD20.3 Syndromes with holoprosencephaly as a major feature
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Any syndrome caused by failure of the prosencephalon to divide in two during the antenatal period. These syndromes may present with closely spaced eyes, cyclopia, flat nasal bridge, single maxillary central incisor, small head size, and clefts of the lip and palate.
code elsewhere
synonyms
- Syndromes with holoprosencephaly as a major feature
- XK aprosencephaly
- Holoprosencephaly - craniosynostosis
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