UMLS 2025C5702219

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	0335U	C5702219	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, fetal sample, identification and categorization of genetic variants	preferred
CPT	0335U	C5702219	RARE DS WHL GEN SEQ FETAL	no pref
CPT	0335U	C5702219	RARE DISEASES WHOLE GENOME SEQ ALYS FETAL SAMPLE	no pref
CPT	0335U	C5702219	Whole genome sequence analysis of fetal sample for detection of abnormalities associated with rare constitutional/heritable diseases	no pref
CPT	0335U	C5702219	Whole genome sequence analysis for detection of 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 in fetal specimen, with identification and categorization of genetic variants associated with rare constitutional and heritable disorders	no pref
HCPT	0335U	C5702219	Whole genome sequence analysis of fetal sample for detection of abnormalities associated with rare constitutional/heritable diseases	no pref
HCPT	0335U	C5702219	Rare ds whl gen seq feta	no pref

Dict

Code

CUI

Term

usa.gov

CPT

0335U

C5702219

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, fetal sample, identification and categorization of genetic variants

preferred

CPT

0335U