UMLS 2025C4732261

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	81443	C4732261	Genetic testing for severe inherited conditions (eg, cystic fibrosis, Ashkenazi Jewish-associated disorders [eg, Bloom syndrome, Canavan disease, Fanconi anemia type C, mucolipidosis type VI, Gaucher disease, Tay-Sachs disease], beta hemoglobinopathies, phenylketonuria, galactosemia), genomic sequence analysis panel, must include sequencing of at least 15 genes (eg, ACADM, ARSA, ASPA, ATP7B, BCKDHA, BCKDHB, BLM, CFTR, DHCR7, FANCC, G6PC, GAA, GALT, GBA, GBE1, HBB, HEXA, IKBKAP, MCOLN1, PAH)	preferred
CPT	81443	C4732261	GENETIC TESTING FOR SEVERE INHERITED CONDITIONS	no pref
CPT	81443	C4732261	GENETIC TSTG SEVERE INH COND	no pref
HCPT	81443	C4732261	Genetic tstg severe inh cond	no pref

Dict

Code

CUI

Term

usa.gov

CPT

81443

C4732261

Genetic testing for severe inherited conditions (eg, cystic fibrosis, Ashkenazi Jewish-associated disorders [eg, Bloom syndrome, Canavan disease, Fanconi anemia type C, mucolipidosis type VI, Gaucher disease, Tay-Sachs disease], beta hemoglobinopathies, phenylketonuria, galactosemia), genomic sequence analysis panel, must include sequencing of at least 15 genes (eg, ACADM, ARSA, ASPA, ATP7B, BCKDHA, BCKDHB, BLM, CFTR, DHCR7, FANCC, G6PC, GAA, GALT, GBA, GBE1, HBB, HEXA, IKBKAP, MCOLN1, PAH)

preferred

CPT

81443