New ICD-10-CM Codes in 2024
327 codes were added to the 2024 ICD-10-CM code set, effective October 1, 2023.
- A41.54 - Sepsis due to Acinetobacter baumannii
- B96.83 - Acinetobacter baumannii as the cause of diseases classified elsewhere
- D13.91 - Familial adenomatous polyposis
- D13.99 - Benign neoplasm of ill-defined sites within the digestive system
- D48.11 - Desmoid tumor
- D48.110 - Desmoid tumor of head and neck
- D48.111 - Desmoid tumor of chest wall
- D48.112 - Desmoid tumor, intrathoracic
- D48.113 - Desmoid tumor of abdominal wall
- D48.114 - Desmoid tumor, intraabdominal
- D48.115 - Desmoid tumor of upper extremity and shoulder girdle
- D48.116 - Desmoid tumor of lower extremity and pelvic girdle
- D48.117 - Desmoid tumor of back
- D48.118 - Desmoid tumor of other site
- D48.119 - Desmoid tumor of unspecified site
- D48.19 - Other specified neoplasm of uncertain behavior of connective and other soft tissue
- D57.04 - Hb-SS disease with dactylitis
- D57.214 - Sickle-cell/Hb-C disease with dactylitis
- D57.414 - Sickle-cell thalassemia, unspecified, with dactylitis
- D57.434 - Sickle-cell thalassemia beta zero with dactylitis
- D57.454 - Sickle-cell thalassemia beta plus with dactylitis
- D57.814 - Other sickle-cell disorders with dactylitis
- D61.02 - Shwachman-Diamond syndrome
- D89.84 - IgG4-related disease
- E20.81 - Hypoparathyroidism due to impaired parathyroid hormone secretion
- E20.810 - Autosomal dominant hypocalcemia
- E20.811 - Secondary hypoparathyroidism in diseases classified elsewhere
- E20.812 - Autoimmune hypoparathyroidism
- E20.818 - Other specified hypoparathyroidism due to impaired parathyroid hormone secretion
- E20.819 - Hypoparathyroidism due to impaired parathyroid hormone secretion, unspecified
- E20.89 - Other specified hypoparathyroidism
- E74.05 - Lysosome-associated membrane protein 2 [LAMP2] deficiency
- E75.27 - Pelizaeus-Merzbacher disease
- E75.28 - Canavan disease
- E79.81 - Aicardi-Goutières syndrome
- E79.82 - Hereditary xanthinuria
- E79.89 - Other specified disorders of purine and pyrimidine metabolism
- E88.43 - Disorders of mitochondrial tRNA synthetases
- E88.810 - Metabolic syndrome
- E88.811 - Insulin resistance syndrome, Type A
- E88.818 - Other insulin resistance
- E88.819 - Insulin resistance, unspecified
- E88.A - Wasting disease (syndrome) due to underlying condition
- G11.5 - Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- G11.6 - Leukodystrophy with vanishing white matter disease
- G20.A - Parkinson's disease without dyskinesia
- G20.A1 - Parkinson's disease without dyskinesia, without mention of fluctuations
- G20.A2 - Parkinson's disease without dyskinesia, with fluctuations
- G20.B - Parkinson's disease with dyskinesia
- G20.B1 - Parkinson's disease with dyskinesia, without mention of fluctuations
- G20.B2 - Parkinson's disease with dyskinesia, with fluctuations
- G20.C - Parkinsonism, unspecified
- G23.3 - Hypomyelination with atrophy of the basal ganglia and cerebellum
- G31.80 - Leukodystrophy, unspecified
- G31.86 - Alexander disease
- G37.81 - Myelin oligodendrocyte glycoprotein antibody disease
- G37.89 - Other specified demyelinating diseases of central nervous system
- G40.C - Lafora progressive myoclonus epilepsy
- G40.C0 - Lafora progressive myoclonus epilepsy, not intractable
- G40.C01 - Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus
- G40.C09 - Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus
- G40.C1 - Lafora progressive myoclonus epilepsy, intractable
- G40.C11 - Lafora progressive myoclonus epilepsy, intractable, with status epilepticus
- G40.C19 - Lafora progressive myoclonus epilepsy, intractable, without status epilepticus
- G43.E - Chronic migraine with aura
- G43.E0 - Chronic migraine with aura, not intractable
- G43.E01 - Chronic migraine with aura, not intractable, with status migrainosus
- G43.E09 - Chronic migraine with aura, not intractable, without status migrainosus
- G43.E1 - Chronic migraine with aura, intractable
- G43.E11 - Chronic migraine with aura, intractable, with status migrainosus
- G43.E19 - Chronic migraine with aura, intractable, without status migrainosus
- G90.B - LMNB1-related autosomal dominant leukodystrophy
- G93.42 - Megaloencephalic leukoencephalopathy with subcortical cysts
- G93.43 - Leukoencephalopathy with calcifications and cysts
- G93.44 - Adult-onset leukodystrophy with axonal spheroids
- H36.8 - Other retinal disorders in diseases classified elsewhere
- H36.81 - Nonproliferative sickle-cell retinopathy
- H36.811 - Nonproliferative sickle-cell retinopathy, right eye
- H36.812 - Nonproliferative sickle-cell retinopathy, left eye
- H36.813 - Nonproliferative sickle-cell retinopathy, bilateral
- H36.819 - Nonproliferative sickle-cell retinopathy, unspecified eye
- H36.82 - Proliferative sickle-cell retinopathy
- H36.821 - Proliferative sickle-cell retinopathy, right eye
- H36.822 - Proliferative sickle-cell retinopathy, left eye
- H36.823 - Proliferative sickle-cell retinopathy, bilateral
- H36.829 - Proliferative sickle-cell retinopathy, unspecified eye
- H36.89 - Other retinal disorders in diseases classified elsewhere
- H50.62 - Inferior oblique muscle entrapment
- H50.621 - Inferior oblique muscle entrapment, right eye
- H50.622 - Inferior oblique muscle entrapment, left eye
- H50.629 - Inferior oblique muscle entrapment, unspecified eye
- H50.63 - Inferior rectus muscle entrapment
- H50.631 - Inferior rectus muscle entrapment, right eye
- H50.632 - Inferior rectus muscle entrapment, left eye
- H50.639 - Inferior rectus muscle entrapment, unspecified eye
- H50.64 - Lateral rectus muscle entrapment
- H50.641 - Lateral rectus muscle entrapment, right eye
- H50.642 - Lateral rectus muscle entrapment, left eye
- H50.649 - Lateral rectus muscle entrapment, unspecified eye
- H50.65 - Medial rectus muscle entrapment