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C3854318

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 81460  C3854318 Whole mitochondrial genome (eg, Leigh syndrome, mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes [MELAS], myoclonic epilepsy with ragged-red fibers [MERFF], neuropathy, ataxia, and retinitis pigmentosa [NARP], Leber hereditary optic neuropathy [LHON]), genomic sequence, must include sequence analysis of entire mitochondrial genome with heteroplasmy detection preferred
 CPT 81460  C3854318 WHOLE MITOCHONDRIAL GENOME no pref
 CPT 81460  C3854318 WHOLE MITOCHONDRIAL GENOME no pref
 HCPT 81460  C3854318 Whole mitochondrial genome no pref
C3854318








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