LD2H
Syndromic genetic deafness
Syndromic genetic deafness
Classification
ICD-11
Chapter
20: Developmental AnomaliesBlock
LD20-LD2ZParent Code
BlockL1-LD2Child Codes
7
WHO Foundation
View on WHOChild Codes (7)
Frequently Asked Questions
What is the ICD-11 code for syndromic genetic deafness?
The ICD-11 code for syndromic genetic deafness is LD2H. The full clinical description is "Syndromic genetic deafness".
What does ICD-11 code LD2H mean?
ICD-11 code LD2H represents “Syndromic genetic deafness”. It is classified under Chapter 20: Developmental Anomalies.
What chapter is LD2H in?
LD2H is in Chapter 20: Developmental Anomalies (codes LA00-LD9Z).
What is the ICD-10 equivalent of ICD-11 code LD2H?
There is no direct ICD-10 mapping available for LD2H 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 LD2H?
LD2H has 7 child codes, including: LD2H.0 (Fraser syndrome), LD2H.1 (Neuropathy with hearing impairment), LD2H.2 (Progressive deafness with stapes fixation), LD2H.3 (Waardenburg-Shah syndrome), and 3 more.
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