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ALL MEDICAL CODES IN CATEGORY Other congenital malformations of the digestive system

2025 ICD-10-CM code Q43.5

Ectopic anus is a congenital malformation where the anus is not in its normal anatomical position.

2025 ICD-10-CM code Q39.5

Congenital dilatation of the esophagus; also known as congenital cardiospasm.

2025 ICD-10-CM code Q43.1

Hirschsprung's disease, also known as aganglionic megacolon, is a congenital condition characterized by the absence of ganglion cells in a segment of the bowel, leading to intestinal obstruction.

2025 ICD-10-CM code Q42

Congenital absence, atresia, and stenosis of the large intestine.

2025 ICD-10-CM code Q40.2

Other specified congenital malformations of the stomach.

2025 ICD-10-CM code Q39

Congenital malformations of the esophagus.

2025 ICD-10-CM code Q45.2

Congenital pancreatic cyst. This condition is present from birth.

2025 ICD-10-CM code Q41.1

Congenital absence, atresia, and stenosis of the jejunum. This includes conditions like apple peel syndrome and imperforate jejunum.

2025 ICD-10-CM code Q44.0

Congenital absence of gallbladder.

2025 ICD-10-CM code Q42.2

Congenital absence, atresia, and stenosis of anus with fistula.

2025 ICD-10-CM code Q38.0

Congenital malformations of lips, not elsewhere classified.

2025 ICD-10-CM code Q38.1

Ankyloglossia (tongue-tie).

2025 ICD-10-CM code Q41.0

Congenital absence, atresia, or stenosis of the duodenum.

2025 ICD-10-CM code Q42.1

Congenital absence, atresia, and stenosis of the rectum without fistula.

2025 ICD-10-CM code Q41.8

Congenital absence, atresia, or stenosis of other specified parts of the small intestine.

2025 ICD-10-CM code Q41

Congenital absence, atresia, and stenosis of the small intestine.

2025 ICD-10-CM code Q45

Other congenital malformations of the digestive system, excluding congenital diaphragmatic hernia and congenital hiatus hernia.

2025 ICD-10-CM code Q44.4

Choledochal cyst

2025 ICD-10-CM code Q42.8

Congenital absence, atresia, and stenosis of other parts of the large intestine.

2025 ICD-10-CM code Q39.0

Atresia of esophagus without fistula. Congenital absence of the normal opening from the esophagus to the stomach.

2025 ICD-10-CM code Q44.6

Cystic disease of liver.This includes fibrocystic disease of the liver.

2025 ICD-10-CM code Q45.1

Annular pancreas. This is a congenital condition where the pancreas forms a ring around the duodenum, the first part of the small intestine.

2025 ICD-10-CM code Q43.2

Other congenital functional disorders of colon. This includes conditions like congenital dilatation of colon.

2025 ICD-10-CM code Q38.4

Congenital malformations of salivary glands and ducts. This includes conditions such as atresia, absence, accessory glands, and fistula.

2025 ICD-10-CM code Q40.3

Congenital malformation of the stomach, unspecified.

2025 ICD-10-CM code Q39.4

Esophageal web, a congenital narrowing of the esophagus.

2025 ICD-10-CM code Q39.6

Congenital diverticulum of the esophagus; a pouch-like protrusion in the esophageal wall present at birth.

2025 ICD-10-CM code Q40.0

Congenital hypertrophic pyloric stenosis, a narrowing of the pylorus (the opening between the stomach and small intestine) in infants, caused by muscle thickening.

2025 ICD-10-CM code Q43.7

Persistent cloaca. Cloaca NOS.

2025 ICD-10-CM code Q44.5

This code describes other congenital malformations of the bile ducts, including accessory hepatic duct, biliary duct duplication, and cystic duct duplication.

2025 ICD-10-CM code Q38

Other congenital malformations of tongue, mouth, and pharynx.

2025 ICD-10-CM code Q43.9

Congenital malformation of intestine, unspecified.

2025 ICD-10-CM code Q42.0

Congenital absence, atresia, and stenosis of the rectum with fistula.

2025 ICD-10-CM code Q44.1

Other congenital malformations of gallbladder.Includes: congenital malformation of gallbladder NOS and intrahepatic gallbladder.

2025 ICD-10-CM code Q40.1

Congenital hiatus hernia. Congenital displacement of cardia through esophageal hiatus.

2025 ICD-10-CM code Q38.5

Congenital malformations of palate, not elsewhere classified. This includes conditions such as congenital absence of uvula and congenital high arched palate.

2025 ICD-10-CM code Q41.9

Congenital absence, atresia, and stenosis of small intestine, part unspecified. This condition involves a lack of development, closure, or narrowing of a portion of the small intestine.

2025 ICD-10-CM code Q39.1

Atresia of esophagus with tracheo-esophageal fistula.This is a birth defect where the esophagus doesn't connect to the stomach, and there's an abnormal connection between the esophagus and trachea.

2025 ICD-10-CM code Q44.2

Atresia of bile ducts.

2025 ICD-10-CM code Q41.2

Congenital absence, atresia, or stenosis of the ileum.

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