LD2F.1
Syndromes with multiple structural anomalies, not of environmental origin
Syndromes with multiple structural anomalies, not of environmental origin
Classification
ICD-11
Chapter
20: Developmental AnomaliesBlock
LD20-LD2ZParent Code
LD2FChild Codes
9
WHO Foundation
View on WHOChild Codes (9)
LD2F.10Prune belly syndrome
LD2F.11VATER association
LD2F.12Sirenomelia
LD2F.13Meckel-Gruber syndrome
LD2F.14MURCS association
LD2F.15Noonan syndrome
LD2F.16Otomandibular dysplasia
LD2F.1YOther specified syndromes with multiple structural anomalies, not of environmental origin
LD2F.1ZSyndromes with multiple structural anomalies, not of environmental origin, unspecified
Frequently Asked Questions
What is the ICD-11 code for syndromes with multiple structural anomalies, not of environmental origin?
The ICD-11 code for syndromes with multiple structural anomalies, not of environmental origin is LD2F.1. The full clinical description is "Syndromes with multiple structural anomalies, not of environmental origin".
What does ICD-11 code LD2F.1 mean?
ICD-11 code LD2F.1 represents “Syndromes with multiple structural anomalies, not of environmental origin”. It is classified under Chapter 20: Developmental Anomalies.
What chapter is LD2F.1 in?
LD2F.1 is in Chapter 20: Developmental Anomalies (codes LA00-LD9Z).
What is the ICD-10 equivalent of ICD-11 code LD2F.1?
There is no direct ICD-10 mapping available for LD2F.1 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 LD2F.1?
LD2F.1 has 9 child codes, including: LD2F.10 (Prune belly syndrome), LD2F.11 (VATER association), LD2F.12 (Sirenomelia), LD2F.13 (Meckel-Gruber syndrome), and 5 more.
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