Excludes2 Notes in Chapter 17: Congenital malformations, deformations and chromosomal abnormalities ICD-10-CM
An Excludes2 note means "NOT INCLUDED HERE": the excluded condition is not part of this code, but a patient may have both, so both codes may be reported. In Chapter 17 (Q00-QA1), notes printed in the chapter name other codes 53 times, and Excludes2 Notes anywhere in the Tabular List name the chapter’s codes 74 times, covering 49 distinct codes, categories and ranges. Switch views to read the list either way.
Excludes2 Notes by the code that carries the note
- Chapter note Chapter 17 (Q00-QA1) Congenital malformations, deformations and chromosomal abnormalities applies to 900 codes
- cleft lip and cleft palate (Q35-Q37)
- congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
- congenital malformation of larynx (Q31.-)
- congenital malformation of lip NEC (Q38.0)
- congenital malformation of nose (Q30.-)
- congenital malformation of parathyroid gland (Q89.2)
- congenital malformation of thyroid gland (Q89.2)
- optic nerve hypoplasia (H47.03-)
- ostium primum atrial septal defect (type I) (Q21.20)
- Q28.8 Other specified congenital malformations of circulatory system
- disorders of pyrophosphate metabolism (E83.82-)
- congenital central alveolar hypoventilation syndrome (G47.35)
- Robin's syndrome (Q87.0)
- congenital myotonic chondrodystrophy (G71.13)
- congenital myotonic chondrodystrophy (G71.13)
- congenital myotonic chondrodystrophy (G71.13)
- Q79 Congenital malformations of musculoskeletal system, not elsewhere classified applies to 14 codes
- congenital (sternomastoid) torticollis (Q68.0)
- Q82.5 Congenital non-neoplastic nevus
- Q82.6 Congenital sacral dimple
- Q82.8 Other specified congenital malformations of skin
- disorders of pyrophosphate metabolism (E83.82-)
- Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified applies to 4 codes
- mitochondrial metabolic disorders (E88.4-)
- multiple endocrine neoplasia [MEN] syndromes (E31.2-)
- Q00-Q99 Anencephaly and similar malformations to Other chromosome abnormalities, not elsewhere classified 882 codes
- Chapter 3 (D50-D89) Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism: congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- Chapter 6 (G00-G99) Diseases of the nervous system: congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- Chapter 7 (H00-H59) Diseases of the eye and adnexa: congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- Chapter 8 (H60-H95) Diseases of the ear and mastoid process: congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- Chapter 9 (I00-I99) Diseases of the circulatory system: congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- Chapter 10 (J00-J99) Diseases of the respiratory system: congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- Chapter 11 (K00-K95) Diseases of the digestive system: congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- Chapter 12 (L00-L99) Diseases of the skin and subcutaneous tissue: congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- Chapter 13 (M00-M99) Diseases of the musculoskeletal system and connective tissue: congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- Chapter 14 (N00-N99) Diseases of the genitourinary system: congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- Chapter 16 (P00-P96) Certain conditions originating in the perinatal period: congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- P04 Newborn affected by noxious substances transmitted via placenta or breast milk: congenital malformations (Q00-Q99)
- Q05.0 Cervical spina bifida with hydrocephalus
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
- Q05.5 Cervical spina bifida without hydrocephalus
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
- Q10.3 Other congenital malformations of eyelid
- L98.7 Excessive and redundant skin and subcutaneous tissue: congenital excess or redundant skin of eyelid (Q10.3)
- Q13.5 Blue sclera
- H15.8 Other disorders of sclera: blue sclera (Q13.5)
- Q14.1 Congenital malformation of retina
- Q20-Q28 Congenital malformations of cardiac chambers and connections to Other congenital malformations of circulatory system 102 codes
- P29 Cardiovascular disorders originating in the perinatal period: congenital malformations of the circulatory system (Q20-Q28)
- Q21.20 Atrioventricular septal defect, unspecified as to partial or complete
- Q21.1 Atrial septal defect: ostium primum atrial septal defect (type I) (Q21.20)
- I08 Multiple valve diseases: multiple valve disease specified as nonrheumatic (I34.-, I35.-, I36.-, I37.-, I38.-, Q22.-, Q23.-, Q24.8-)
- Q23.0 Congenital stenosis of aortic valve
- I35 Nonrheumatic aortic valve disorders: aortic valve disorder specified as congenital (Q23.0, Q23.1)
- Q23.1 Congenital insufficiency of aortic valve
- I35 Nonrheumatic aortic valve disorders: aortic valve disorder specified as congenital (Q23.0, Q23.1)
- I08 Multiple valve diseases: multiple valve disease specified as nonrheumatic (I34.-, I35.-, I36.-, I37.-, I38.-, Q22.-, Q23.-, Q24.8-)
- Q24.5 Malformation of coronary vessels
- Q27 Other congenital malformations of peripheral vascular system: anomalies of coronary vessels (Q24.5)
- Q24.8- Other specified congenital malformations of heart
- I08 Multiple valve diseases: multiple valve disease specified as nonrheumatic (I34.-, I35.-, I36.-, I37.-, I38.-, Q22.-, Q23.-, Q24.8-)
- Q25.5-Q25.7 Atresia of pulmonary artery to Other congenital malformations of pulmonary artery 5 codes
- Q27 Other congenital malformations of peripheral vascular system: anomalies of pulmonary artery (Q25.5-Q25.7)
- Q25.79 Other congenital malformations of pulmonary artery
- Q28 Other congenital malformations of circulatory system: congenital pulmonary aneurysm (Q25.79)
- I72 Other aneurysm: aneurysm (of) arteriovenous NOS (Q27.3-)
- Q27.8 Other specified congenital malformations of peripheral vascular system
- Q28 Other congenital malformations of circulatory system: congenital peripheral aneurysm (Q27.8)
- Q28.0 Arteriovenous malformation of precerebral vessels
- Q27.3 Arteriovenous malformation (peripheral): arteriovenous malformation of precerebral vessels (Q28.0)
- Q28.0-Q28.3 Arteriovenous malformation of precerebral vessels to Other malformations of cerebral vessels 4 codes
- Q27 Other congenital malformations of peripheral vascular system: anomalies of cerebral and precerebral vessels (Q28.0-Q28.3)
- Q28.1 Other malformations of precerebral vessels
- Q28.2 Arteriovenous malformation of cerebral vessels
- Q27.3 Arteriovenous malformation (peripheral): arteriovenous malformation of cerebral vessels (Q28.2)
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: congenital malformation of nose (Q30.-)
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: congenital malformation of larynx (Q31.-)
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: cleft lip and cleft palate (Q35-Q37)
- Q38.0 Congenital malformations of lips, not elsewhere classified
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: congenital malformation of lip NEC (Q38.0)
- Q38.2 Macroglossia
- K14 Diseases of tongue: macroglossia (congenital) (Q38.2)
- Q40.0 Congenital hypertrophic pyloric stenosis
- Block R10-R19 Symptoms and signs involving the digestive system and abdomen: congenital or infantile pylorospasm (Q40.0)
- Q40.1 Congenital hiatus hernia
- Q45 Other congenital malformations of digestive system: congenital hiatus hernia (Q40.1)
- Q44.6 Cystic disease of liver
- K76 Other diseases of liver: cystic disease of liver (congenital) (Q44.6)
- Q62.0-Q62.3 Congenital hydronephrosis to Other obstructive defects of renal pelvis and ureter 8 codes
- N13 Obstructive and reflux uropathy: congenital obstructive defects of renal pelvis and ureter (Q62.0-Q62.3)
- Q62.11 Congenital occlusion of ureteropelvic junction
- N13 Obstructive and reflux uropathy: hydronephrosis with ureteropelvic junction obstruction (Q62.11)
- Q65-Q79 Congenital deformities of hip to Congenital malformations of musculoskeletal system, not elsewhere classified 255 codes
- M95 Other acquired deformities of musculoskeletal system and connective tissue: congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
- Q67.5 Congenital deformity of spine
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
- Q68.0 Congenital deformity of sternocleidomastoid muscle
- Q79 Congenital malformations of musculoskeletal system, not elsewhere classified: congenital (sternomastoid) torticollis (Q68.0)
- Q74.3 Arthrogryposis multiplex congenita
- Q76.0-Q76.4 Spina bifida occulta to Other congenital malformations of spine, not associated with scoliosis 16 codes
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
- Q79.0 Congenital diaphragmatic hernia
- Q45 Other congenital malformations of digestive system: congenital diaphragmatic hernia (Q79.0)
- Block E70-E88 Metabolic disorders: Ehlers-Danlos syndromes (Q79.6-)
- M35.7 Hypermobility syndrome: Ehlers-Danlos syndromes (Q79.6-)
- Q79.8 Other congenital malformations of musculoskeletal system
- Q83 Congenital malformations of breast: absence of pectoral muscle (Q79.8)
- Q82.1 Xeroderma pigmentosum
- G11.3 Cerebellar ataxia with defective DNA repair: xeroderma pigmentosum (Q82.1)
- Q82.5 Congenital non-neoplastic nevus
- D18 Hemangioma and lymphangioma, any site: vascular nevus (Q82.5)
- I78.1 Nevus, non-neoplastic: flammeus nevus (Q82.5)
- I78.1 Nevus, non-neoplastic: portwine nevus (Q82.5)
- I78.1 Nevus, non-neoplastic: sanguineous nevus (Q82.5)
- I78.1 Nevus, non-neoplastic: strawberry nevus (Q82.5)
- I78.1 Nevus, non-neoplastic: verrucous nevus (Q82.5)
- Q82.6 Congenital sacral dimple
- Q07 Other congenital malformations of nervous system: neurofibromatosis (nonmalignant) (Q85.0-)
- Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
- Block Q35-Q37 Cleft lip and cleft palate: Robin's syndrome (Q87.0)
- Q87.11 Prader-Willi syndrome
- E66 Overweight and obesity: Prader-Willi syndrome (Q87.11)
- Q87.19 Other congenital malformation syndromes predominantly associated with short stature
- G11.3 Cerebellar ataxia with defective DNA repair: Cockayne's syndrome (Q87.19)
- Q87.2 Congenital malformation syndromes predominantly involving limbs
- N07 Hereditary nephropathy, not elsewhere classified: nail patella syndrome (Q87.2)
- Q87.81- Alport syndrome
- N07 Hereditary nephropathy, not elsewhere classified: Alport's syndrome (Q87.81-)
- Q89.2 Congenital malformations of other endocrine glands
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: congenital malformation of parathyroid gland (Q89.2)
- Block Q10-Q18 Congenital malformations of eye, ear, face and neck: congenital malformation of thyroid gland (Q89.2)
The first view lists notes printed in this chapter (a note on a category or block applies to every code beneath it). The second lists codes of this chapter named by Excludes2 Notes anywhere in the Tabular List, including notes in other chapters.
Questions About Excludes2 Notes
What does an Excludes2 note mean?
An Excludes2 note means “Not included here”: the excluded condition is not part of the condition represented by the code, but a patient may have both conditions at the same time (Section I.A.12.b). The FY 2027 Tabular List has 2,529 of them; 2,493 name other codes, with 2,799 references to 1,779 distinct codes, categories and ranges.
Can both codes be reported when there is an Excludes2 note?
Yes. When an Excludes2 note appears under a code, it is acceptable to use both the code and the excluded code together, when appropriate: that is, when the patient has both conditions and both are documented.
Related References
Source: FY 2027 ICD-10-CM Tabular List (CMS and NCHS) and the ICD-10-CM Official Guidelines for Coding and Reporting FY 2027, Section I.A. ICD List is not affiliated with CMS or NCHS.