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ALL MEDICAL CODES IN CATEGORY Other congenital malformations of the digestive system (Q38-Q45)

2025 ICD-10-CM code Q38.8

Other congenital malformations of the pharynx.

2025 ICD-10-CM code Q40.8

Other specified congenital malformations of upper alimentary tract.

2025 ICD-10-CM code Q38

Other congenital malformations of tongue, mouth, and pharynx.

2025 ICD-10-CM code Q43.0

Meckel's diverticulum (displaced) (hypertrophic). Persistent omphalomesenteric duct. Persistent vitelline duct.

2025 ICD-10-CM code Q43.8

Other specified congenital malformations of intestine.

2025 ICD-10-CM code Q39.8

Other congenital malformations of esophagus.Includes: congenital absence of esophagus, congenital displacement of esophagus, congenital duplication of esophagus.

2025 ICD-10-CM code Q40.9

Congenital malformation of the upper alimentary tract, unspecified.

2025 ICD-10-CM code Q45.9

Congenital malformation of the digestive system, unspecified.

2025 ICD-10-CM code Q43.9

Congenital malformation of intestine, unspecified.

2025 ICD-10-CM code Q42.3

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

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 Q42.9

Congenital absence, atresia, and stenosis of large intestine, part unspecified.

2025 ICD-10-CM code Q44

Congenital malformations of the gallbladder, bile ducts, and liver.

2025 ICD-10-CM code Q44.7

Other congenital malformations of the liver. This code also includes, if applicable, associated malformations affecting other systems.

2025 ICD-10-CM code Q45.0

Congenital absence of pancreas. This code encompasses agenesis, aplasia, and hypoplasia of the pancreas.

2025 ICD-10-CM code Q39.9

Congenital malformation of esophagus, unspecified.

2025 ICD-10-CM code Q39.2

Congenital tracheo-esophageal fistula without atresia.