Revised ICD-10-CM Codes in 2024 

Revised ICD-10-CM Codes in 2024 

26 code descriptions were revised in the 2024 ICD-10-CM code set, effective October 1, 2023.

Displaying codes 1-26 of 26:

1. H54.511  Low vision, right eye, category 1
   • Old long description: Low vision, right eye, category 1-2
   • Old short description: Low vision, right eye, category 1-2
2. I25.112  Atherosclerotic heart disease of native coronary artery with refractory angina pectoris
   • Old long description: Atherosclerosic heart disease of native coronary artery with refractory angina pectoris
   • Old short description: Atherosclerosic hrt dis of natv cor art w refract ang pctrs
3. I71.51  Supraceliac aneurysm of the thoracoabdominal aorta, ruptured
   • Old long description: Supraceliac aneurysm of the abdominal aorta, ruptured
   • Old short description: Supraceliac aneurysm of the abdominal aorta, ruptured
4. I71.52  Paravisceral aneurysm of the thoracoabdominal aorta, ruptured
   • Old long description: Paravisceral aneurysm of the abdominal aorta, ruptured
   • Old short description: Paravisceral aneurysm of the abdominal aorta, ruptured
5. I71.61  Supraceliac aneurysm of the thoracoabdominal aorta, without rupture
   • Old long description: Supraceliac aneurysm of the abdominal aorta, without rupture
   • Old short description: Supraceliac aneurysm of the abdominal aorta, without ruptur
6. I71.62  Paravisceral aneurysm of the thoracoabdominal aorta, without rupture
   • Old long description: Paravisceral aneurysm of the abdominal aorta, without rupture
   • Old short description: Paravisceral aneurysm of the abd aorta, without rupture
7. M32.15  Tubulo-interstitial nephropathy in systemic lupus erythematosus
   • Old long description: Tubulo-interstitial nephropathy in systemic lupus erythematosus
   • Old short description: Tubulo-interstitial neuropath in sys lupus erythematosus
8. M41.12  Adolescent idiopathic scoliosis
   • Old long description: Adolescent scoliosis
   • Old short description: Adolescent scoliosis
9. N07.1  Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
   • Old long description: Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
   • Old short description: Heredit neuropath, NEC w focal and seg glomerular lesions
10. N07.3  Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
    • Old long description: Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
    • Old short description: Heredit neuropath, NEC w diffuse mesangial prolif glomrlnep
11. N07.4  Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
    • Old long description: Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
    • Old short description: Heredit neuropath, NEC w diffus endocaplry prolif glomrlnep
12. N13.721  Vesicoureteral-reflux with reflux nephropathy without hydroureter, unilateral
    • Old long description: Vesicoureteral-reflux with reflux nephropathy without hydroureter, unilateral
    • Old short description: Vesicoureter-reflux w reflux neuropath w/o hydrourt, unil
13. N13.722  Vesicoureteral-reflux with reflux nephropathy without hydroureter, bilateral
    • Old long description: Vesicoureteral-reflux with reflux nephropathy without hydroureter, bilateral
    • Old short description: Vesicoureter-reflux w reflux neuropath w/o hydrourt, bi
14. N13.731  Vesicoureteral-reflux with reflux nephropathy with hydroureter, unilateral
    • Old long description: Vesicoureteral-reflux with reflux nephropathy with hydroureter, unilateral
    • Old short description: Vesicoureter-reflux w reflux neuropath w hydrourt, unil
15. N13.732  Vesicoureteral-reflux with reflux nephropathy with hydroureter, bilateral
    • Old long description: Vesicoureteral-reflux with reflux nephropathy with hydroureter, bilateral
    • Old short description: Vesicoureter-reflux w reflux neuropath w hydrourt, bilatera
16. N14.2  Nephropathy induced by unspecified drug, medicament or biological substance
    • Old long description: Nephropathy induced by unspecified drug, medicament or biological substance
    • Old short description: Neuropath induced by unsp drug, medicament or biolg sub
17. N35.812  Other bulbous urethral stricture, male
    • Old long description: Other urethral bulbous stricture, male
    • Old short description: Other urethral bulbous stricture, male
18. P19.9  Metabolic acidemia in newborn, unspecified
    • Old long description: Metabolic acidemia, unspecified
    • Old short description: Metabolic acidemia, unspecified
19. Q85.81  PTEN hamartoma tumor syndrome
    • Old long description: PTEN tumor syndrome
    • Old short description: PTEN tumor syndrome
20. Q87.4  Marfan syndrome
    • Old long description: Marfan’s syndrome
    • Old short description: Marfan’s syndrome
21. Q87.40  Marfan syndrome, unspecified
    • Old long description: Marfan’s syndrome, unspecified
    • Old short description: Marfan’s syndrome, unspecified
22. Q87.41  Marfan syndrome with cardiovascular manifestations
    • Old long description: Marfan’s syndrome with cardiovascular manifestations
    • Old short description: Marfan’s syndrome with cardiovascular manifestations
23. Q87.410  Marfan syndrome with aortic dilation
    • Old long description: Marfan’s syndrome with aortic dilation
    • Old short description: Marfan’s syndrome with aortic dilation
24. Q87.418  Marfan syndrome with other cardiovascular manifestations
    • Old long description: Marfan’s syndrome with other cardiovascular manifestations
    • Old short description: Marfan’s syndrome with other cardiovascular manifestations
25. Q87.42  Marfan syndrome with ocular manifestations
    • Old long description: Marfan’s syndrome with ocular manifestations
    • Old short description: Marfan’s syndrome with ocular manifestations
26. Q87.43  Marfan syndrome with skeletal manifestation
    • Old long description: Marfan’s syndrome with skeletal manifestation
    • Old short description: Marfan’s syndrome with skeletal manifestation