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C5691532

ICD-10 (International Classification of Diseases, 10th Revision)
ICD-10 is split into two systems for use in the U.S.:
CPT (Current Procedural Terminology)
HCPCS (Healthcare Common Procedure Coding System)
HCPT (HCPCS Version of Current Procedural Terminology).HCPT is another name for the HCPCS Level I set.


Enter one or more words or parts of words
   

Dict Code CUI Term usa.gov
 CPT 0273U  C5691532 HEM GEN HYPRFIBRNLYSIS 9 GEN no pref
 CPT 0273U  C5691532 Genomic sequence analysis of 9 genes for detection of abnormalities associated with genetic hyperfibrinolysis and delayed bleeding no pref
 CPT 0273U  C5691532 Hematology (genetic hyperfibrinolysis, delayed bleeding), analysis of 9 genes (F13A1, F13B, FGA, FGB, FGG, SERPINA1, SERPINE1, SERPINF2 by next-generation sequencing, and PLAU by array comparative genomic hybridization), blood, buccal swab, or amniotic fluid preferred
 CPT 0273U  C5691532 HEM GEN HYPRFIBRNLYSIS DLYD BLD ALYS 9 GEN no pref
 HCPT 0273U  C5691532 Hem gen hyprfibrnlysis 8 gen no pref
 HCPT 0273U  C5691532 Genomic sequence analysis of 9 genes for detection of abnormalities associated with genetic hyperfibrinolysis and delayed bleeding no pref
C5691532








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