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WELCOME

Procedure Code Category	CPT Codes	Procedure Code Descriptions	Code Status
SPLE	38102	Splenectomy; total, en bloc for extensive disease, in conjunction with other procedure (List in No changeition to code for primary procedure)	No Change
SPLE	38115	Repair of ruptured spleen (splenorrhaphy) with or without partial splenectomy	No Change
SPLE	38120	Laparoscopy, surgical, splenectomy	No Change
THOR	20101	Exploration of penetrating wound (separate procedure); chest	No Change
THOR	21603	Excision of chest wall tumor involving rib(s), with plastic reconstruction; with mediastinal lymphadenectomy	No change
THOR	31770	Bronchoplasty; graft repair	No Change
THOR	31775	Bronchoplasty; excision stenosis and anastomosis	No Change
THOR	32096	Thoracotomy, with diagnostic biopsy(ies) of lung infiltrate(s) (eg, wedge, incisional), unilateral	No Change
THOR	32097	Thoracotomy, with diagnostic biopsy(ies) of lung nodule(s) or mass(es) (eg, wedge, incisional), unilateral	No Change
THOR	32100	Thoracotomy; with exploration	No Change
THOR	32110	Thoracotomy; with control of traumatic hemorrhage and/or repair of lung tear	No Change
THOR	32120	Thoracotomy; for postoperative complications	No Change

CPT CODE	PROCEDURE	PRICE
76770	US RENAL with Doppler with 93975	0
76536	US Soft Tissue Neck (thyroid, parathyroid, etc.)	0
76870	US TESTICULAR	0
76870	US TESTICULAR with Doppler with 93975	0
76536	US THYROID	0
10005	US THYROID FNA/FINE NEEDLE ASPIRATION	0
0	including Ultrasound Guidance - First lesion\	0
10006	US THYROID FNA/FINE NEEDLE ASPIRATION -	0
0	additional lesions	0
76776	US TRANSPLANTED KIDNEY	0
NUCLEAR	0	0
CPT CODE	PROCEDURE	PRICE

TEST ID	Test Name	CPT Code
GNF13	Factor XIII Deficiency, F13A1 and F13B Genes, Next-Generation Sequencing, Varies	81479 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)
GNFIB	Congenital Fibrinogen Disorders, FGA, FGB, and FGG Genes, Next-Generation Sequencing, Varies	81479 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)
GNPRC	Protein C Deficiency, PROC Gene, Next-Generation Sequencing, Varies	81479
GNPRS	Protein S Deficiency, PROS1 Gene, Next-Generation Sequencing, Varies	81479
GNVWD	von Willebrand Disease, VWF and GP1BA Genes, Next-Generation Sequencing, Varies	81408 81479 81479 (if appropriate for government payers) 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)
GNANG	Hereditary Angioedema Focused Gene Panel, Next-Generation Sequencing, Varies	81479
GNADM	Hereditary Thrombotic Thrombocytopenic Purpura, ADAMTS13 Gene, Next-Generation Sequencing, Varies	81479
GNBLF	Bleeding Disorders, Focused Gene Panel, Next-Generation Sequencing, Varies	81238 81407 81408 81479 81479 (if appropriate for government payers) 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)
GNBLC	Bleeding Disorders, Comprehensive Gene Panel, Next-Generation Sequencing, Varies	81443 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)
GNTHR	Thrombosis Disorders, Comprehensive Gene Panel, Next-Generation Sequencing, Varies	81443
GNPLT	Platelet Disorders, Comprehensive Gene Panel, Next-Generation Sequencing, Varies	81443 88233-Tissue culture, skin, solid tissue biopsy (if appropriate) 88240-Cryopreservation (if appropriate)
GNMY9	MYH9-Related Disorders, MYH9 Gene, Next-Generation Sequencing, Varies	81479

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