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C3511554

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 81326  C3511554 PMP22 GENE ANALYSIS KNOWN FAMILIAL VARIANT no pref
 CPT 81326  C3511554 PMP22 GENE KNOWN FAM VARIANT no pref
 CPT 81326  C3511554 PMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary neuropathy with liability to pressure palsies) gene analysis; known familial variant preferred
 HCPT 81326  C3511554 Pmp22 gene known fam variant no pref
 CPT 81326  C3511554 Peripheral myelin protein 22 (PMP22) gene analysis for known familial variant no pref
C3511554








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