Home

             UMLS 2025

7/10

C4051854

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 81434  C4051854 Hereditary retinal disorders (eg, retinitis pigmentosa, Leber congenital amaurosis, cone-rod dystrophy), genomic sequence analysis panel, must include sequencing of at least 15 genes, including ABCA4, CNGA1, CRB1, EYS, PDE6A, PDE6B, PRPF31, PRPH2, RDH12, RHO, RP1, RP2, RPE65, RPGR, and USH2A preferred
 CPT 81434  C4051854 HEREDITARY RTA DO GEN SEQ ALYS AT LEAST 15 GEN no pref
 CPT 81434  C4051854 HERED RTA DO GEN SEQ 15 no pref
 HCPT 81434  C4051854 Hered rta do gen seq 15 no pref
C4051854








Read more: https://www.nlm.nih.gov/research/umls/sourcereleasedocs/


Web development by Gayane Margaryan