E27.49
BillableOther adrenocortical insufficiency
Other adrenocortical insufficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Adrenal hemorrhage
- Adrenal infarction
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(1)
Also Known As / Clinical Terms(181)
SNOMED CT
- Adrenal calcification12286000
- Hypocortisolism secondary to another disorder16685009
- Secondary adrenal insufficiency16685009
- Secondary adrenocortical insufficiency16685009
- Secondary hypocortisolism16685009
- Achalasia-addisonian syndrome45414006
- Alacrimia-achalasia-addisonianism45414006
- Allgrove syndrome45414006
- Glucocorticoid deficiency with achalasia45414006
- Triple A syndrome45414006
- Achalasia of cardia45564002
- Achalasia of esophagus45564002
- Achalasia of oesophagus45564002
- Cardiospasm45564002
- Lack of reflex relaxation of lower esophageal sphincter45564002
- Lack of reflex relaxation of lower oesophageal sphincter45564002
- Adrenal haemorrhage49111001
- Adrenal hemorrhage49111001
- Aldosterone deficiency60086000
- Hypoaldosteronism60086000
- Isolated ACTH deficiency80599001
- Isolated corticotropin deficiency80599001
- Specific corticotropin deficiency80599001
- Adrenal infarction85096001
- Hyperkalaemic renal tubular acidosis236463002
- Hyperkalemic renal tubular acidosis236463002
- RTA (renal tubular acidosis) type IV236463002
- Renal tubular acidosis type 4236463002
- Type IV renal tubular acidosis236463002
- Hyporeninaemic hypoaldosteronism236464008
- Hyporeninemic hypoaldosteronism236464008
- RTH (resistance to thyroid hormone) syndrome237559000
- Resistance to TH (thyroid hormone) syndrome237559000
- Resistance to thyroid hormone syndrome237559000
- Thyroid hormone resistance237559000
- Thyroid hormone resistance syndrome237559000
- ACTH deficiency237692001
- Adrenocorticotropic hormone (ACTH) deficiency237692001
- Adrenocorticotropic hormone deficiency237692001
- Secondary hypoadrenalism237692001
- Adrenal insufficiency due to adrenal metastasis237761007
- Hyperreninaemic hypoaldosteronism237765003
- Hyperreninemic hypoaldosteronism237765003
- Adrenocortical haemorrhage237766002
- Adrenocortical hemorrhage237766002
- Adrenal atrophy237772002
- Injury of adrenal gland262831009
- Injury of suprarenal gland262831009
- Adrenal gland haematoma262832002
- Adrenal gland hematoma262832002
- Adrenal necrosis308894004
- Pituitary thyroid hormone resistance360348000
- Primary adrenocortical insufficiency373662000
- Primary hypoadrenalism373662000
- Congenital achalasia of esophagus700283004
- Congenital achalasia of oesophagus700283004
- Familial aldosterone deficiency715343000
- Familial hypoaldosteronism715343000
- Hereditary glucocorticoid resistance715402001
- Generalised glucocorticoid resistance syndrome819950002
- Generalized glucocorticoid resistance syndrome819950002
- Autonomic neuropathy due to Allgrove syndrome838322007
- ACTH (adrenocorticotropic hormone) resistance syndrome1156181008
- Adrenocorticotropic hormone insensitivity1156181008
- Adrenocorticotropic hormone resistance syndrome1156181008
- Adrenocorticotropin resistance syndrome1156181008
- Hypoadrenalism due to paracoccidioidomycosis1163509008
- Familial hyperreninaemic hypoaldosteronism type 21186812001
- Familial hyperreninemic hypoaldosteronism type 21186812001
- Adrenal cortical hypofunction due to interruption of corticosteroid therapy1186858000
- Adrenal cortex atrophy1217048002
- Adrenocortical atrophy1217048002
- Atrophy of adrenal cortex1217048002
- Adrenal degeneration1217055000
- Degeneration of adrenal gland1217055000
- Familial hyperreninaemic hypoaldosteronism type 1B1217069000
- Familial hyperreninemic hypoaldosteronism type 1B1217069000
- Familial hyperreninaemic hypoaldosteronism type 1A1217075009
- Familial hyperreninemic hypoaldosteronism type 1A1217075009
- Congenital isolated ACTH (adrenocorticotropic hormone) deficiency1231283007
- Congenital isolated adrenocorticotropic hormone deficiency1231283007
- Mineralocorticoid deficiency7651000119100
UMLS
- Adrenal HemorrhageC0151693
- Adrenal bleedingC0151693
- Adrenal haemorrhageC0151693
- Adrenal hemorrhageC0151693
- Adrenal hemorrhage (disorder)C0151693
- Haemorrhage adrenalC0151693
- Hemorrhage adrenalC0151693
- adrenal haemorrhageC0151693
- adrenal hemorrhageC0151693
- Adrenal infarctionC0271751
- Adrenal infarction (disorder)C0271751
- Other adrenocortical insufficiencyC2874196
Clinical Terms
- Adrenal gland hematoma
- Familial hyperreninaemic hypoaldosteronism type 1B
- ACTH deficiency
- Adrenal insufficiency due to adrenal metastasis
- Atrophy of adrenal cortex
- RTA (renal tubular acidosis) type IV
- Congenital achalasia of oesophagus
- Achalasia-addisonian syndrome
- Primary hypoadrenalism
- Familial hyperreninemic hypoaldosteronism type 1A
- Haemorrhage adrenal
- Adrenal atrophy
- Adrenal degeneration
- Familial aldosterone deficiency
- Hereditary glucocorticoid resistance
- Renal tubular acidosis type 4
- Adrenocorticotropic hormone deficiency
- Secondary hypoadrenalism
- Injury of suprarenal gland
- Isolated ACTH deficiency
- Adrenal cortex atrophy
- Lack of reflex relaxation of lower esophageal sphincter
- Lack of reflex relaxation of lower oesophageal sphincter
- Familial hyperreninaemic hypoaldosteronism type 2
- Pituitary thyroid hormone resistance
- adrenal hemorrhage
- Triple A syndrome
- Congenital isolated ACTH (adrenocorticotropic hormone) deficiency
- Primary adrenocortical insufficiency
- Adrenal necrosis
- Adrenal hemorrhage (disorder)
- Thyroid hormone resistance syndrome
- Adrenocorticotropic hormone insensitivity
- Alacrimia-achalasia-addisonianism
- Familial hyperreninemic hypoaldosteronism type 1B
- Secondary adrenocortical insufficiency
- Achalasia of cardia
- Adrenal bleeding
- Isolated corticotropin deficiency
- Adrenocortical hemorrhage
- Familial hyperreninemic hypoaldosteronism type 2
- Generalized glucocorticoid resistance syndrome
- Glucocorticoid deficiency with achalasia
- Specific corticotropin deficiency
- Adrenocortical haemorrhage
- Adrenal infarction
- Familial hyperreninaemic hypoaldosteronism type 1A
- Congenital isolated adrenocorticotropic hormone deficiency
- Degeneration of adrenal gland
- Achalasia of oesophagus
- Adrenal infarction (disorder)
- Hyporeninaemic hypoaldosteronism
- Achalasia of esophagus
- Adrenocorticotropic hormone (ACTH) deficiency
- Familial hypoaldosteronism
- Adrenocorticotropin resistance syndrome
- Hypocortisolism secondary to another disorder
- Aldosterone deficiency
- Hypoaldosteronism
- Resistance to TH (thyroid hormone) syndrome
- Hyperkalaemic renal tubular acidosis
- Hyperreninaemic hypoaldosteronism
- Hypoadrenalism due to paracoccidioidomycosis
- Hyperkalemic renal tubular acidosis
- Adrenocorticotropic hormone resistance syndrome
- Cardiospasm
- Secondary hypocortisolism
- Adrenocortical atrophy
- Hemorrhage adrenal
- Secondary adrenal insufficiency
- Mineralocorticoid deficiency
- Type IV renal tubular acidosis
- adrenal haemorrhage
- Adrenal calcification
- Congenital achalasia of esophagus
- RTH (resistance to thyroid hormone) syndrome
- Hyperreninemic hypoaldosteronism
- Autonomic neuropathy due to Allgrove syndrome
- Injury of adrenal gland
- ACTH (adrenocorticotropic hormone) resistance syndrome
- Allgrove syndrome
- Generalised glucocorticoid resistance syndrome
- Adrenal gland haematoma
- Thyroid hormone resistance
- Adrenal cortical hypofunction due to interruption of corticosteroid therapy
- Resistance to thyroid hormone syndrome
- Hyporeninemic hypoaldosteronism
Frequently Asked Questions
What is the ICD-10 code for other adrenocortical insufficiency?
The ICD-10-CM code for other adrenocortical insufficiency is E27.49. The full clinical description is "Other adrenocortical insufficiency". E27.49 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E27.49 mean?
ICD-10-CM code E27.49 represents “Other adrenocortical insufficiency”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E27.49 a billable code?
Yes, E27.49 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E27.49 in?
E27.49 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E27.49?
E27.49 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); galactorrhea (N64.3); gynecomastia (N62); and 2 more.
What SNOMED CT codes does E27.49 map to?
E27.49 maps to 36 SNOMED CT concepts: 1156181008, 237692001, 45564002, 45414006, 237772002, and 31 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E27.49?
E27.49 is linked to 3 UMLS Concept Unique Identifiers: C0151693, C0271751, C2874196. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E27.49 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other adrenocortical insufficiency affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E27.49?
There is no direct ICD-11 mapping available for E27.49 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.