C5164248

UMLS CUI C5164248 is "F9 gene mutation analysis limited to known familial mutations | Amniotic fluid or Chorionic villus sample | Mutations".

F9 gene mutation analysis limited to known familial mutations | Amniotic fluid or Chorionic villus sample | Mutations (CUI C5164248) groups: 1 LOINC code.

The Unified Medical Language System is the NLM's meta-terminology that unifies SNOMED CT, ICD-10, ICD-11, RxNorm, LOINC, MeSH, and around 200 other source vocabularies under a single concept identifier (CUI). One UMLS CUI can group dozens of synonymous codes from different terminologies.

A CUI is a stable identifier (like C0011860) that points at a single clinical idea regardless of how that idea is encoded in any specific vocabulary. CUIs are the most reliable way to bridge between terminologies when you need to compare or merge data from multiple sources.

Every UMLS concept page lists the codes it groups together. That gives you a free crosswalk: a SNOMED concept and an ICD-10 code that share a CUI describe the same clinical idea. Our cross_references API returns these groupings inline.

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