Other diseases of esophagus (K22)
K22 codes cover a variety of less common conditions affecting the esophagus, ranging from obstructions and ulcers to motility disorders and Barrett's esophagus. These ICD-10 codes are essential for specifying precise diagnoses related to esophageal disease beyond more typical reflux conditions.
The K22.0 code captures achalasia of the cardia, a disorder also known as "absence of peristalsis" or "idiopathic achalasia," characterized by impaired esophageal muscle movement and difficulty swallowing. Ulcers of the esophagus are classified under K22.1, with or without bleeding (K22.10 and K22.11), including causes such as infections, medication, or corrosive injury. Obstruction of the esophagus (K22.2) covers a range of strictures and webs that narrow the esophagus, while perforation (K22.3) refers to esophageal tears or ruptures needing urgent attention. Dyskinesia (K22.4) includes motility disorders like nutcracker esophagus and diffuse spasm. Barrett's esophagus is tracked by codes K22.7 through K22.719, separating cases with or without dysplasia, an important precancerous condition. Acquired diverticula (K22.5) and gastro-esophageal lacerations or hemorrhage (K22.6, known as Mallory-Weiss syndrome) are also specified. Other less common or unspecified esophageal conditions fall under K22.8 and K22.9. These ICD-10 codes for other diseases of esophagus support accurate documentation of complex esophageal disorders for both clinical and billing purposes.
Diseases of the digestive system (K00–K95)
Diseases of esophagus, stomach and duodenum (K20-K31)
K22 Other diseases of esophagus
- K22.0 Achalasia of cardia
K22.1 Ulcer of esophagus
- K22.10 Ulcer of esophagus without bleeding
- K22.11 Ulcer of esophagus with bleeding
- K22.2 Esophageal obstruction
- K22.3 Perforation of esophagus
- K22.4 Dyskinesia of esophagus
- K22.5 Diverticulum of esophagus, acquired
- K22.6 Gastro-esophageal laceration-hemorrhage syndrome
K22.7 Barrett's esophagus
- K22.70 Barrett's esophagus without dysplasia
K22.71 Barrett's esophagus with dysplasia
- K22.710 Barrett's esophagus with low grade dysplasia
- K22.711 Barrett's esophagus with high grade dysplasia
- K22.719 Barrett's esophagus with dysplasia, unspecified
K22.8 Other specified diseases of esophagus
- K22.81 Esophageal polyp
- K22.82 Esophagogastric junction polyp
- K22.89 Other specified disease of esophagus
- K22.9 Disease of esophagus, unspecified
Other diseases of esophagus (K22)
Instructional Notations
Type 2 Excludes
A type 2 excludes note represents "Not included here". An excludes2 note indicates that the condition excluded is not part of the condition represented by the code, but a patient may have both conditions at the same time. When an Excludes2 note appears under a code, it is acceptable to use both the code and the excluded code together, when appropriate.
- esophageal varices I85
Clinical Terms
The following clinical terms provide additional context, helping users better understand the clinical background and common associations for each diagnosis listed in this section. Including related terms alongside ICD-10-CM codes supports coders, billers, and healthcare professionals in improving accuracy, enhancing documentation, and facilitating research or patient education.
Esophageal Fistula
Abnormal passage communicating with the ESOPHAGUS. The most common type is TRACHEOESOPHAGEAL FISTULA between the esophagus and the TRACHEA.
Moyamoya Disease
A noninflammatory, progressive occlusion of the intracranial CAROTID ARTERIES and the formation of netlike collateral arteries arising from the CIRCLE OF WILLIS. Cerebral angiogram shows the puff-of-smoke (moyamoya) collaterals at the base of the brain. It is characterized by endothelial HYPERPLASIA and FIBROSIS with thickening of arterial walls. This disease primarily affects children but can also occur in adults.
Thyroid Hormone Resistance Syndrome
An inherited autosomal recessive trait, characterized by peripheral resistance to THYROID HORMONES and the resulting elevation in serum levels of THYROXINE and TRIIODOTHYRONINE. This syndrome is caused by mutations of gene THRB encoding the THYROID HORMONE RECEPTORS BETA in target cells. HYPOTHYROIDISM in these patients is partly overcome by the increased thyroid hormone levels.