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WELCOME

Procedure Code Category	CPT Codes	Procedure Code Descriptions	Code Status
SB	44312	Revision of ileostomy; simple (release of superficial scar) (separate procedure)	No Change
SB	44314	Revision of ileostomy; complicated (reconstruction in-depth) (separate procedure)	No Change
SB	44316	Continent ileostomy (Kock procedure) (separate procedure)	No Change
SB	44602	Suture of small intestine (enterorrhaphy) for perforated ulcer, diverticulum, wound, injury or rupture; single perforation	No Change
SB	44603	Suture of small intestine (enterorrhaphy) for perforated ulcer, diverticulum, wound, injury or rupture; multiple perforations	No Change
SB	44615	Intestinal stricturoplasty (enterotomy and enterorrhaphy) with or without dilation, for intestinal obstruction	No Change
SB	44640	Closure of intestinal cutaneous fistula	No Change
SB	44650	Closure of enteroenteric or enterocolic fistula	No Change
SB	44800	Excision of Meckel's diverticulum (diverticulectomy) or omphalomesenteric duct	No Change
SB	45136	Excision of ileoanal reservoir with ileostomy	No Change
SPLE	38100	Splenectomy; total (separate procedure)	No Change
SPLE	38101	Splenectomy; partial (separate procedure)	No Change

CPT CODE	PROCEDURE	PRICE
76705	US INGUINAL CANAL	0
76817	US OB 1st TRIMESTER TRANSVAGINAL	0
76801	US OB FIRST TRIMESTER	0
76812	US OB FIRST TRIMESTER - additional fetus	0
76536	US PARATHYROID	0
76856	US PELVIS MALE	0
76830	US PELVIS - TRANSVAGINAL	0
76830	US PELVIS - TRANSVAGINAL with Doppler with 93975	0
76856	US PELVIS - NON OB	0
76857	US PELVIS - NON OB LIMITED	0
76856	US PELVIS - NON OB with Doppler with 93975	0
76770	US RENAL	0

TEST ID	Test Name	CPT Code
NCYB	Recessive Congenital Methemoglobinemia, CYB5 and CYB5 Reductase Genetic Analysis, Next-Generation Sequencing, Varies	81479
NHEM	Hereditary Erythrocytosis Focused Gene Panel, Next-Generation Sequencing, Varies	81404 81479 81479 (if appropriate for government payers)
GNANT	Antithrombin Deficiency, SERPINC1 Gene, Next-Generation Sequencing, Varies	81479
NHEP	Hereditary Erythrocytosis Gene Panel, Next-Generation Sequencing, Varies	81404 81405 81479 81479 (if appropriate for government payers)
NHHA	Hereditary Hemolytic Anemia Gene Panel, Next-Generation Sequencing, Varies	81443
NENZ	Red Blood Cell Enzyme Disorders Gene Panel, Next-Generation Sequencing, Varies	81443
NMEM	Red Blood Cell Membrane Disorders Gene Panel, Next-Generation Sequencing, Varies	81405 81479 81479 (if appropriate for government payers)
NCDA	Congenital Dyserythropoietic Anemia Gene Panel, Next-Generation Sequencing, Varies	81479
GNF7	Factor VII Deficiency, F7 Gene, Next-Generation Sequencing, Varies	81479 88233-Tissue culture, skin, solid tissue biopsy (if appropriate) 88240-Cryopreservation (if appropriate) 88235-Amniotic fluid culture (if appropriate)
GNHMA	Hemophilia A, F8 Gene, Next-Generation Sequencing, Varies	81407 88233-Tissue culture, skin, solid tissue biopsy (if appropriate) 88240-Cryopreservation (if appropriate) 88235-Amniotic fluid culture (if appropriate) 81265-Maternal cell contamination (if appropriate)
GNHMB	Hemophilia B, F9 Gene, Next-Generation Sequencing, Varies	81238 88233-Tissue culture, skin, solid tissue biopsy (if appropriate) 88240-Cryopreservation (if appropriate) 88235-Amniotic fluid culture (if appropriate) 81265-Maternal cell contamination (if appropriate)
GNF11	Hemophilia C (Factor XI Deficiency), F11 Gene, Next-Generation Sequencing, Varies	81479 88233-Tissue culture, skin, solid tissue biopsy (if appropriate) 88240-Cryopreservation (if appropriate) 88235-Amniotic fluid culture (if appropriate)

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