UMLS 2025C5702220

ICD-10 (International Classification of Diseases, 10th Revision)
ICD-10 is split into two systems for use in the U.S.:

ICD-10-CM: Clinical Modification codes (3 to 7 characters) are used by all healthcare settings to report a patient's diseases, injuries, signs, and symptoms (e.g., diagnosis of pneumonia or a broken arm).
ICD-10-PCS: Procedure Coding System codes (7 alphanumeric characters) are used only in inpatient hospital settings to report procedures performed (e.g., removing a tumor).

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.


CPT	0336U	C5702220	RARE DISEASES WHOLE GENOME SEQ ALYS BLOOD/SALIVA	no pref
CPT	0336U	C5702220	Rare diseases (constitutional/heritable disorders), whole genome sequence analysis, including small sequence changes, copy number variants, deletions, duplications, mobile element insertions, uniparental disomy (UPD), inversions, aneuploidy, mitochondrial genome sequence analysis with heteroplasmy and large deletions, short tandem repeat (STR) gene expansions, blood or saliva, identification and categorization of genetic variants, each comparator genome (eg, parent)	preferred
CPT	0336U	C5702220	RARE DS WHL GEN SEQ BLD/SLV	no pref
HCPT	0336U	C5702220	Rare ds whl gen seq bld/slv	no pref

Dict

Code

CUI

Term

usa.gov

CPT

0336U

C5702220

RARE DISEASES WHOLE GENOME SEQ ALYS BLOOD/SALIVA

no pref

CPT

0336U