E16.4
BillableIncreased secretion of gastrin
Increased secretion of gastrin
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hypergastrinemia
- Hyperplasia of pancreatic endocrine cells with gastrin excess
- Zollinger-Ellison syndrome
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
Also Known As / Clinical Terms
SNOMED CT
- Hyperplasia of islet alpha cells with gastrin excess1051005
- Familial hypergastrinaemic duodenal ulcer6761005
- Familial hypergastrinemic duodenal ulcer6761005
- Islet cell hyperplasia42681006
- Nesidioblastosis42681006
- Pancreatic endocrine cell hyperplasia42681006
- Abnormality of secretion of gastrin47344007
- Excessive gastrin secretion53132006
- ZE - Zollinger-Ellison syndrome53132006
- Zollinger-Ellison syndrome53132006
- Abnormal hormone secretion53439008
- Disorder of hormone secretion53439008
- Megaloblastic anaemia due to Zollinger-Ellison syndrome54698001
- Megaloblastic anemia due to Zollinger-Ellison syndrome54698001
- Impaired acid inhibition of gastrin release56497004
- G cell tumor302824004
- G cell tumour302824004
- Gastrinoma302824004
- Drug-induced hypergastrinaemia717889000
- Drug-induced hypergastrinemia717889000
- Hypergastrinaemia caused by drug717889000
- Hypergastrinemia caused by drug717889000
- Anastomotic ulcer due to Zollinger-Ellison syndrome717890009
- Gastric ulcer due to Zollinger-Ellison syndrome717891008
- Duodenal ulcer due to Zollinger-Ellison syndrome717892001
- Cancerous ulcer870711002
- Malignant ulcer870711002
- Ulcer due to cancer870711002
- Hypergastrinaemia367641000119101
- Hypergastrinemia367641000119101
- Increased gastrin secretion367641000119101
UMLS
- Excessive gastrin secretionC0043515
- Syndrome Zollinger EllisonC0043515
- Syndrome, Zollinger-EllisonC0043515
- Z-E syndromeC0043515
- ZE - Zollinger-Ellison syndromeC0043515
- Zollinger Ellison SyndromeC0043515
- Zollinger Ellison syndromeC0043515
- Zollinger-Ellison SyndromeC0043515
- Zollinger-Ellison syndromeC0043515
- Zollinger-Ellison syndrome (disorder)C0043515
- ellison syndrome zollingerC0043515
- gastrinoma syndromeC0043515
- syndrome gastrinomaC0043515
- syndrome z-eC0043515
- syndrome zollinger ellisonC0043515
- syndrome zollinger ellisonsC0043515
- syndrome zollinger-ellisonC0043515
- ulcerogenic tumor of the pancreas syndromeC0043515
- z-e syndromeC0043515
- zollinger ellison syndromeC0043515
- zollinger-ellison syndromeC0043515
- HypergastrinaemiaC0232567
- HypergastrinemiaC0232567
- Increased gastrin secretionC0232567
- Increased gastrin secretion (disorder)C0232567
- hypergastrinaemiaC0232567
- hypergastrinemiaC0232567
- Hyperplasia of pancreatic endocrine cells with gastrin excessC2874180
- Increased secretion of gastrinC2874181
Frequently Asked Questions
What is ICD-10 code E16.4?
ICD-10-CM code E16.4 represents "Increased secretion of gastrin". It is a billable/specific code that can be used on a claim.
Is E16.4 a billable code?
Yes, E16.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E16.4 in?
E16.4 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E16.4?
E16.4 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74).
What SNOMED CT codes does E16.4 map to?
E16.4 maps to 15 SNOMED CT concepts: 53439008, 47344007, 717890009, 870711002, 717889000, and 10 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E16.4?
E16.4 is linked to 4 UMLS Concept Unique Identifiers: C0043515, C0232567, C2874180, C2874181. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.