LD24.G
Syndromic craniosynostoses
Syndromic craniosynostoses
Classification
ICD-11
Chapter
20: Developmental AnomaliesBlock
LD20-LD2ZParent Code
LD24Child Codes
5
WHO Foundation
View on WHOChild Codes (5)
Frequently Asked Questions
What is the ICD-11 code for syndromic craniosynostoses?
The ICD-11 code for syndromic craniosynostoses is LD24.G. The full clinical description is "Syndromic craniosynostoses".
What does ICD-11 code LD24.G mean?
ICD-11 code LD24.G represents “Syndromic craniosynostoses”. It is classified under Chapter 20: Developmental Anomalies.
What chapter is LD24.G in?
LD24.G is in Chapter 20: Developmental Anomalies (codes LA00-LD9Z).
What is the ICD-10 equivalent of ICD-11 code LD24.G?
There is no direct ICD-10 mapping available for LD24.G in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-10. Use the ICD-11 to ICD-10 converter to search for related codes.
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.
What are the subcategories under LD24.G?
LD24.G has 5 child codes, including: LD24.G0 (Pfeiffer syndrome), LD24.G1 (Crouzon disease), LD24.G2 (Apert syndrome), LD24.GY (Other specified syndromic craniosynostoses), and 1 more.
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