LD50.01
Karyotype 46, X iso Xq
Karyotype 46, X iso Xq
Classification
ICD-11
Chapter
20: Developmental AnomaliesBlock
LD50-LD5ZParent Code
LD50.0ICD-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(3)
Frequently Asked Questions
What is the ICD-11 code for karyotype 46, x iso xq?
The ICD-11 code for karyotype 46, x iso xq is LD50.01. The full clinical description is "Karyotype 46, X iso Xq".
What does ICD-11 code LD50.01 mean?
ICD-11 code LD50.01 represents “Karyotype 46, X iso Xq”. It is classified under Chapter 20: Developmental Anomalies.
What chapter is LD50.01 in?
LD50.01 is in Chapter 20: Developmental Anomalies (codes LA00-LD9Z).
What is the ICD-10 equivalent of ICD-11 code LD50.01?
LD50.01 maps to the ICD-10 code: Q96.1 (Karyotype 46, X iso (Xq)). 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.
What SNOMED CT codes does LD50.01 map to?
LD50.01 maps to 2 SNOMED CT concepts: 38804009, 205686009. SNOMED CT is a clinical terminology used in electronic health records.
What UMLS concepts map to ICD-11 code LD50.01?
LD50.01 is linked to 1 UMLS Concept Unique Identifier: C2910375. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.