From: Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study
Diagnosis | ICD-9-CM | ICD-10-CM |
 Carrier of genetic disease | V83.89 | Z14.8 |
 Genetic susceptibility to or family history of cancer | V84.09 | Z15.09 |
Procedure | ICD-9-CMa | CPT |
 Abdominal Ultrasound |  | 76700, 76770 |
 CA 125 |  | 86304 |
 Colectomy | 17.33–17.36, 45.73–45.76, 45.81, 45.82, 45.93 | 44140, 44141, 44152, 44204, 44310 |
 Colonoscopy | 45.21, 45.23, 45.24, 45.42, 48.23 | G0105, G0121, 44388, 45300, 45305, 45331, 45378, 45380, 45381, 45385, 45386 |
 EGD/Endoscopy | 45.13, 45.16 | 43259, 43752, 43234 |
 Endometrial Biopsy |  | 57505, 58100 |
 Pelvic Ultrasound |  | 76856 |
 Genetic Counseling |  | 96040 |
 Hysterectomy | 68.3, 68.41, 68.49, 68.59 | 58150, 58180, 58260, 58571, 58573 |
 Oophorectomy | 65.61, 65.63, 65.64 | 58720, 58951, 58952 |
 Transvaginal Ultrasound |  | 76817, 76830, 76857 |
 Urinalysis |  | 81000–81003, 81015, 81099 |