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DC32.2 Hereditary chronic pancreatitis International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01 Hereditary chronic pancreatitis is a very rare form of childhood onset chronic pancreatitis. With the exception of an earlier onset and a slower progression the clinical course, the morphological features and laboratory findings of HCP do not differ from those present in patients with alcoholic chronic pancreatitis.
postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed [select] ME24 Clinical manifestations of the digestive system – ME24.0 Digestive system abscess – ME24.1 Digestive system fistula – ME24.2 Digestive system obstruction – ME24.3 Digestive system perforation – ME24.4 Digestive system stenosis – ME24.5 Digestive system ulcer – ME24.6 Digestive system dilatation – ME24.7 Digestive system incarceration – ME24.8 Digestive system strangulation or gangrene – ME24.9 Gastrointestinal bleeding – ME24.A Other digestive system haemorrhage, not elsewhere classified – ME24.Y Other specified clinical manifestations of the digestive system –– ME24.30 Perforation of small intestine –– ME24.31 Perforation of large intestine –– ME24.35 Perforation of gallbladder or bile ducts –– ME24.3Y Digestive system perforation of other specified site –– ME24.3Z Digestive system perforation of unspecified site –– ME24.90 Acute gastrointestinal bleeding, not elsewhere classified –– ME24.91 Chronic gastrointestinal bleeding, not elsewhere classified –– ME24.9Z Gastrointestinal bleeding, unspecified –– ME24.A0 Obscure gastrointestinal bleeding –– ME24.A1 Haemorrhage of anus and rectum –– ME24.A2 Oesophageal haemorrhage –– ME24.A3 Haematochezia –– ME24.A4 Melaena –– ME24.A5 Haematemesis –– ME24.A6 Positive occult blood in stool ––– MG30.42 Chronic visceral pain from persistent inflammation Associated with - multiple selections are allowed [select] 5A10 Type 1 diabetes mellitus 5A11 Type 2 diabetes mellitus 5A12 Malnutrition-related diabetes mellitus 5A13 Diabetes mellitus, other specified type – 5A13.0 Diabetes mellitus due to genetic defects of beta cell function – 5A13.1 Diabetes mellitus due to genetic defects in insulin action – 5A13.2 Diabetes mellitus due to diseases of the exocrine pancreas – 5A13.3 Diabetes mellitus due to endocrinopathies – 5A13.4 Diabetes mellitus due to drug or chemical – 5A13.5 Diabetes mellitus due to uncommon forms of immune-mediated diabetes – 5A13.6 Diabetes mellitus due to other genetic syndromes – 5A13.7 Diabetes mellitus due to clinically defined subtypes or syndromes – 5A13.Y Diabetes mellitus due to other specified cause 5A14 Diabetes mellitus, type unspecified – 5A20 Diabetic hyperosmolar hyperglycaemic state –– 5A20.0 Hyperosmolar hyperglycaemic state without coma –– 5A20.1 Hyperosmolar hyperglycaemic state with coma –– 5A20.Z Diabetic hyperosmolar hyperglycaemic state, unspecified – 5A21 Hypoglycaemia in the context of diabetes mellitus –– 5A21.0 Hypoglycaemia in the context of diabetes mellitus without coma –– 5A21.1 Hypoglycaemia in the context of diabetes mellitus with coma –– 5A21.Z Hypoglycaemia in the context of diabetes, unspecified – 5A22 Diabetic acidosis –– 5A22.0 Diabetic ketoacidosis without coma –– 5A22.1 Diabetic lactic acidosis –– 5A22.2 Diabetic metabolic acidosis –– 5A22.3 Diabetic ketoacidosis with coma –– 5A22.Y Other specified diabetic acidosis –– 5A22.Z Diabetic acidosis, unspecified – 5A23 Diabetic coma – 5A24 Uncontrolled or unstable diabetes mellitus – 5A2Y Other specified acute complications of diabetes mellitus
synonyms Hereditary chronic pancreatitis
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