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C3248154

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 81243  C3248154 FMR1 GENE ALYS EVAL TO DETECT ABNORMAL ALLELES no pref
 CPT 81243  C3248154 Fragile X messenger ribonucleoprotein 1 gene analysis evaluation to detect abnormal alleles no pref
 CPT 81243  C3248154 FMR1 (fragile X messenger ribonucleoprotein 1) (eg, fragile X syndrome, X-linked intellectual disability [XLID]) gene analysis; evaluation to detect abnormal (eg, expanded) alleles preferred
 CPT 81243  C3248154 FMR1 GEN ALY DETC ABNL ALLEL no pref
 CPT 81243  C3248154 FMR1 gene analysis evaluation to detect abnormal alleles no pref
 HCPT 81243  C3248154 Fmr1 gen aly detc abnl allel no pref
C3248154








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