Autoimmune Addison disease
Congenital small adrenal gland
Steroid-resistant nephrotic syndrome
Adrenal Insufficiency, Primary
Muscle disorders associated with endocrine disease
Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency
Hypocortisolism
Primary hypoadrenalism
Primary adrenocortical failure
primary adrenal insufficiency
Melanosis of mucosa of body orifice
Addison's disease due to autoimmunity (disorder)
Disease Addison's
Autoimmune Addison's disease
Pituitary thyroid hormone resistance
CAH - Congenital adrenal hypoplasia
Addison disease
Hypoadrenalism, Primary
Thyroid hormone resistance syndrome
Adrenocorticotropic hormone insensitivity
Primary adrenocortical insufficiency (disorder)
Congenital primary adrenocortical hypofunction
Addisons Disease
Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
Congenital hypoplasia of adrenal gland
autoimmune adrenalitis
Hyperpigmentation of oral mucosa
Classic Addison disease
Primary immunodeficiency due to MCM4 (mini-chromosome maintenance complex component 4) deficiency
Congenital adrenal hypoplasia
Hypoadrenalisms, Primary
Disease, Addison
Adrenocorticotropin resistance syndrome
Steroid-unresponsive nephrotic syndrome
Chronic Primary Adrenal Insufficiency
Endocrine myopathy
Adrenocortical Insufficiencies, Primary
Congenital Addison disease
Hereditary adrenal unresponsiveness to corticotropin
Resistance to TH (thyroid hormone) syndrome
Buccal pigmentation due to Addison disease
addison's disease
Primary adrenal insufficiency, steroid-resistant nephrotic syndrome due to SGPL1 (sphingosine-1-phosphate lyase 1) deficiency
Buccal pigmentation due to Addison's disease
ADDISONS DIS
Familial glucocorticoid deficiency
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency
Insufficiencies, Primary Adrenocortical
Adrenocorticotropic hormone resistance syndrome
Addison's disease (disorder)
Primary immunodeficiency due to MCM4 deficiency
Addison's disease due to autoimmunity
Autoimmune Primary Adrenal Insufficiency
adrenalitis
Adrenal insufficiency (Addison disease)
Insufficiency, Primary Adrenocortical
Addison disease due to autoimmunity
SRNS - Steroid-resistant nephrotic syndrome
Adrenocortical Insufficiency, Primary
ADDISON DIS
Primary adrenal insufficiency, steroid-resistant nephrotic syndrome due to SGPL1 deficiency
RTH (resistance to thyroid hormone) syndrome
Muscle disease related to endocrine disease
Adrenomyodystrophy
ACTH (adrenocorticotropic hormone) resistance syndrome
Mucosal melanosis
Autoimmune adrenal atrophy
Thyroid hormone resistance
Primary Adrenocortical Insufficiencies
Myopathy in Addison's disease
Myopathy in Addison disease
Primary Addison disease
Melanin pigmentation of oral mucosa
Resistance to thyroid hormone syndrome

Frequently Asked Questions

What is the ICD-10 code for primary adrenocortical insufficiency?

The ICD-10-CM code for primary adrenocortical insufficiency is E27.1. The full clinical description is "Primary adrenocortical insufficiency". E27.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E27.1 mean?

ICD-10-CM code E27.1 represents “Primary 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 E27.1 a billable code?

Yes, E27.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E27.1 in?

E27.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E27.1?

E27.1 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 4 more.

What SNOMED CT codes does E27.1 map to?

E27.1 maps to 20 SNOMED CT concepts: 1156181008, 363732003, 76715008, 763311001, 403252006, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E27.1?

E27.1 is linked to 3 UMLS Concept Unique Identifiers: C0001403, C0271737, C5848257. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E27.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like primary 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 E27.1?

E27.1 maps to the ICD-11 code: 5A74.0 (Acquired adrenocortical insufficiency).

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try Free View API Docs

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.