LA05.2
Holoprosencephaly
Holoprosencephaly
Classification
ICD-11
Chapter
20: Developmental AnomaliesBlock
LA00-LA0ZParent Code
LA05ICD-10 Mapping
1 equivalentWHO Foundation
View on WHOICD-10 Equivalents(1)
ICD-10 Equivalents
View full mappingCorresponding ICD-10-CM codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(10)
SNOMED CT ↗
- Familial alobar holoprosencephaly30915001
- Congenital absence of pancreas82949000
- Cebocephalus204052006
- Agenesis of pancreas204806003
- Cingulosynapsis253136007
- Alobar holoprosencephaly253137003
- Congenital stenosis of nasal pyriform aperture702644002
- Camero Lituania Cohen syndrome715434005
- Agnathia, holoprosencephaly, situs inversus syndrome722283003
- Aplasia of pancreas1144555008
Frequently Asked Questions
What is the ICD-11 code for holoprosencephaly?
The ICD-11 code for holoprosencephaly is LA05.2. The full clinical description is "Holoprosencephaly".
What does ICD-11 code LA05.2 mean?
ICD-11 code LA05.2 represents “Holoprosencephaly”. It is classified under Chapter 20: Developmental Anomalies.
What chapter is LA05.2 in?
LA05.2 is in Chapter 20: Developmental Anomalies (codes LA00-LD9Z).
What is the ICD-10 equivalent of ICD-11 code LA05.2?
LA05.2 maps to the ICD-10 code: Q04.2 (Holoprosencephaly). This is an equivalent mapping.
What is the difference between ICD-10 and ICD-11?
ICD-11 is the latest revision of the WHO's International Classification of Diseases, succeeding ICD-10. Key differences include: a fully digital-first design, new chapters for sleep-wake disorders, sexual health, and traditional medicine, improved coding for rare diseases, and better integration with electronic health records through extension codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.