15,083 codes
CC codes (complication or comorbidity)
Secondary diagnoses that raise an inpatient stay to the middle-severity MS-DRG in a family, unless excluded for the principal diagnosis. Source: MS-DRG v44 Definitions Manual, Appendix C.
Chapter 17: Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders
- Q01.0Frontal encephalocele
- Q01.1Nasofrontal encephalocele
- Q01.2Occipital encephalocele
- Q01.8Encephalocele of other sites
- Q01.9Encephalocele, unspecified
- Q04.4Septo-optic dysplasia of brain
- Q04.5Megalencephaly
- Q04.6Congenital cerebral cysts
- Q04.8Other specified congenital malformations of brain
- Q05.0Cervical spina bifida with hydrocephalus
- Q05.1Thoracic spina bifida with hydrocephalus
- Q05.2Lumbar spina bifida with hydrocephalus
- Q05.3Sacral spina bifida with hydrocephalus
- Q05.4Unspecified spina bifida with hydrocephalus
- Q07.02Arnold-Chiari syndrome with hydrocephalus
- Q07.03Arnold-Chiari syndrome with spina bifida and hydrocephalus
- Q20.5Discordant atrioventricular connection
- Q21.0Ventricular septal defect
- Q21.10Atrial septal defect, unspecified
- Q21.11Secundum atrial septal defect
- Q21.12Patent foramen ovale
- Q21.13Coronary sinus atrial septal defect
- Q21.14Superior sinus venosus atrial septal defect
- Q21.15Inferior sinus venosus atrial septal defect
- Q21.16Sinus venosus atrial septal defect, unspecified
- Q21.19Other specified atrial septal defect
- Q21.20Atrioventricular septal defect, unspecified as to partial or complete
- Q21.21Partial atrioventricular septal defect
- Q21.22Transitional atrioventricular septal defect
- Q21.23Complete atrioventricular septal defect
- Q22.1Congenital pulmonary valve stenosis
- Q22.2Congenital pulmonary valve insufficiency
- Q22.3Other congenital malformations of pulmonary valve
- Q23.0Congenital stenosis of aortic valve
- Q23.1Congenital insufficiency of aortic valve
- Q23.2Congenital mitral stenosis
- Q23.3Congenital mitral insufficiency
- Q24.0Dextrocardia
- Q24.1Levocardia
- Q24.3Pulmonary infundibular stenosis
- Q24.5Malformation of coronary vessels
- Q25.0Patent ductus arteriosus
- Q25.1Coarctation of aorta
- Q25.21Interruption of aortic arch
- Q25.29Other atresia of aorta
- Q25.3Supravalvular aortic stenosis
- Q25.40Congenital malformation of aorta unspecified
- Q25.41Absence and aplasia of aorta
- Q25.42Hypoplasia of aorta
- Q25.43Congenital aneurysm of aorta
- Q25.44Congenital dilation of aorta
- Q25.45Double aortic arch
- Q25.46Tortuous aortic arch
- Q25.47Right aortic arch
- Q25.48Anomalous origin of subclavian artery
- Q25.49Other congenital malformations of aorta
- Q25.8Other congenital malformations of other great arteries
- Q25.9Congenital malformation of great arteries, unspecified
- Q26.0Congenital stenosis of vena cava
- Q26.1Persistent left superior vena cava
- Q26.2Total anomalous pulmonary venous connection
- Q26.3Partial anomalous pulmonary venous connection
- Q26.4Anomalous pulmonary venous connection, unspecified
- Q26.8Other congenital malformations of great veins
- Q26.9Congenital malformation of great vein, unspecified
- Q27.30Arteriovenous malformation, site unspecified
- Q27.4Congenital phlebectasia
- Q28.0Arteriovenous malformation of precerebral vessels
- Q28.1Other malformations of precerebral vessels
- Q28.8Other specified congenital malformations of circulatory system
- Q28.9Congenital malformation of circulatory system, unspecified
- Q31.1Congenital subglottic stenosis
- Q31.2Laryngeal hypoplasia
- Q31.3Laryngocele
- Q31.5Congenital laryngomalacia
- Q31.8Other congenital malformations of larynx
- Q31.9Congenital malformation of larynx, unspecified
- Q32.0Congenital tracheomalacia
- Q32.1Other congenital malformations of trachea
- Q32.2Congenital bronchomalacia
- Q32.3Congenital stenosis of bronchus
- Q32.4Other congenital malformations of bronchus
- Q33.0Congenital cystic lung
- Q33.4Congenital bronchiectasis
- Q39.5Congenital dilatation of esophagus
- Q39.6Congenital diverticulum of esophagus
- Q39.8Other congenital malformations of esophagus
- Q39.9Congenital malformation of esophagus, unspecified
- Q41.0Congenital absence, atresia and stenosis of duodenum
- Q41.1Congenital absence, atresia and stenosis of jejunum
- Q41.2Congenital absence, atresia and stenosis of ileum
- Q41.8Congenital absence, atresia and stenosis of other specified parts of small intestine
- Q41.9Congenital absence, atresia and stenosis of small intestine, part unspecified
- Q42.0Congenital absence, atresia and stenosis of rectum with fistula
- Q42.1Congenital absence, atresia and stenosis of rectum without fistula
- Q42.2Congenital absence, atresia and stenosis of anus with fistula
- Q42.3Congenital absence, atresia and stenosis of anus without fistula
- Q42.8Congenital absence, atresia and stenosis of other parts of large intestine
- Q42.9Congenital absence, atresia and stenosis of large intestine, part unspecified
- Q43.1Hirschsprung's disease
- Q43.2Other congenital functional disorders of colon
- Q43.3Congenital malformations of intestinal fixation
- Q43.4Duplication of intestine
- Q43.5Ectopic anus
- Q43.6Congenital fistula of rectum and anus
- Q43.7Persistent cloaca
- Q43.8Other specified congenital malformations of intestine
- Q43.9Congenital malformation of intestine, unspecified
- Q44.0Agenesis, aplasia and hypoplasia of gallbladder
- Q44.1Other congenital malformations of gallbladder
- Q44.4Choledochal cyst
- Q44.5Other congenital malformations of bile ducts
- Q44.6Cystic disease of liver
- Q44.70Other congenital malformation of liver, unspecified
- Q44.71Alagille syndrome
- Q44.79Other congenital malformations of liver
- Q45.0Agenesis, aplasia and hypoplasia of pancreas
- Q45.1Annular pancreas
- Q45.2Congenital pancreatic cyst
- Q45.3Other congenital malformations of pancreas and pancreatic duct
- Q60.0Renal agenesis, unilateral
- Q60.1Renal agenesis, bilateral
- Q60.2Renal agenesis, unspecified
- Q60.3Renal hypoplasia, unilateral
- Q60.4Renal hypoplasia, bilateral
- Q60.5Renal hypoplasia, unspecified
- Q60.6Potter's syndrome
- Q61.00Congenital renal cyst, unspecified
- Q61.01Congenital single renal cyst
- Q61.02Congenital multiple renal cysts
- Q61.11Cystic dilatation of collecting ducts
- Q61.19Other polycystic kidney, infantile type
- Q61.2Polycystic kidney, adult type
- Q61.3Polycystic kidney, unspecified
- Q61.4Renal dysplasia
- Q61.5Medullary cystic kidney
- Q61.8Other cystic kidney diseases
- Q61.9Cystic kidney disease, unspecified
- Q62.0Congenital hydronephrosis
- Q62.10Congenital occlusion of ureter, unspecified
- Q62.11Congenital occlusion of ureteropelvic junction
- Q62.12Congenital occlusion of ureterovesical orifice
- Q62.2Congenital megaureter
- Q62.31Congenital ureterocele, orthotopic
- Q62.32Cecoureterocele
- Q62.39Other obstructive defects of renal pelvis and ureter
- Q64.10Exstrophy of urinary bladder, unspecified
- Q64.11Supravesical fissure of urinary bladder
- Q64.12Cloacal exstrophy of urinary bladder
- Q64.19Other exstrophy of urinary bladder
- Q64.2Congenital posterior urethral valves
- Q64.31Congenital bladder neck obstruction
- Q64.32Congenital stricture of urethra
- Q64.33Congenital stricture of urinary meatus
- Q64.39Other atresia and stenosis of urethra and bladder neck
- Q67.5Congenital deformity of spine
- Q67.8Other congenital deformities of chest
- Q68.1Congenital deformity of finger(s) and hand
- Q74.3Arthrogryposis multiplex congenita
- Q76.3Congenital scoliosis due to congenital bony malformation
- Q76.425Congenital lordosis, thoracolumbar region
- Q76.426Congenital lordosis, lumbar region
- Q76.427Congenital lordosis, lumbosacral region
- Q76.428Congenital lordosis, sacral and sacrococcygeal region
- Q76.429Congenital lordosis, unspecified region
- Q76.6Other congenital malformations of ribs
- Q76.7Congenital malformation of sternum
- Q76.8Other congenital malformations of bony thorax
- Q76.9Congenital malformation of bony thorax, unspecified
- Q77.2Short rib syndrome
- Q78.0Osteogenesis imperfecta
- Q78.2Osteopetrosis
- Q79.60Ehlers-Danlos syndrome, unspecified
- Q79.61Classical Ehlers-Danlos syndrome
- Q79.62Hypermobile Ehlers-Danlos syndrome
- Q79.63Vascular Ehlers-Danlos syndrome
- Q79.69Other Ehlers-Danlos syndromes
- Q85.1Tuberous sclerosis
- Q85.81PTEN hamartoma tumor syndrome
- Q85.82Other Cowden syndrome
- Q85.83Von Hippel-Lindau syndrome
- Q85.89Other phakomatoses, not elsewhere classified
- Q85.9Phakomatosis, unspecified
- Q87.11Prader-Willi syndrome
- Q87.19Other congenital malformation syndromes predominantly associated with short stature
- Q87.2Congenital malformation syndromes predominantly involving limbs
- Q87.3Congenital malformation syndromes involving early overgrowth
- Q87.40Marfan syndrome, unspecified
- Q87.410Marfan syndrome with aortic dilation
- Q87.418Marfan syndrome with other cardiovascular manifestations
- Q87.42Marfan syndrome with ocular manifestations
- Q87.43Marfan syndrome with skeletal manifestation
- Q87.5Other congenital malformation syndromes with other skeletal changes
- Q87.81Alport syndrome
- Q87.82Arterial tortuosity syndrome
- Q87.83Bardet-Biedl syndrome
- Q87.84Laurence-Moon syndrome
- Q87.85MED13L syndrome
- Q87.86Kleefstra syndrome
- Q87.87Hao-Fountain Syndrome
- Q87.88CTNNB1 syndrome
- Q87.89Other specified congenital malformation syndromes, not elsewhere classified
- Q87.ALoeys-Dietz syndrome
- Q89.01Asplenia (congenital)
- Q89.09Congenital malformations of spleen
- Q89.3Situs inversus
- Q89.7Multiple congenital malformations, not elsewhere classified
- Q89.81Kabuki syndrome
- Q89.89Other specified congenital malformations
- Q91.0Trisomy 18, nonmosaicism (meiotic nondisjunction)
- Q91.1Trisomy 18, mosaicism (mitotic nondisjunction)
- Q91.2Trisomy 18, translocation
- Q91.3Trisomy 18, unspecified
- Q91.4Trisomy 13, nonmosaicism (meiotic nondisjunction)
- Q91.5Trisomy 13, mosaicism (mitotic nondisjunction)
- Q91.6Trisomy 13, translocation
- Q91.7Trisomy 13, unspecified
- Q93.3Deletion of short arm of chromosome 4
- Q93.4Deletion of short arm of chromosome 5
- Q93.51Angelman syndrome
- Q93.52Phelan-McDermid syndrome
- Q93.59Other deletions of part of a chromosome
- Q93.7Deletions with other complex rearrangements
- Q93.82Williams syndrome
- Q93.88Other microdeletions
- Q93.89Other deletions from the autosomes
- Q93.9Deletion from autosomes, unspecified
- Q99.811Usher syndrome, type 1
- Q99.812Usher syndrome, type 2
- Q99.813Usher syndrome, type 3
- Q99.818Other Usher syndrome
- Q99.819Usher syndrome, unspecified
- QA0.0101SCN2A-related neurodevelopmental disorder
- QA0.0102CACNA1A-related neurodevelopmental disorder
- QA0.0109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
- QA0.011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
- QA0.012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
- QA0.0131SLC6A1-related disorder
- QA0.0139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
- QA0.0141Syntaxin-binding protein 1-related disorder
- QA0.0142DLG4-related synaptopathy
- QA0.0149Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
- QA0.0151FOXG1 syndrome
- QA0.0159Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
- QA0.8Other neurodevelopmental disorders related to pathogenic variants in other specific genes