E22.0
BillableAcromegaly and pituitary gigantism
Acromegaly and pituitary gigantism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Overproduction of growth hormone
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •galactorrheaN64.3
- •gynecomastiaN62
- •Cushing's syndromeE24
- •Nelson's syndromeE24.1
- •overproduction of ACTH not associated with Cushing's diseaseE27.0
- •overproduction of pituitary ACTHE24.0
- •overproduction of thyroid-stimulating hormoneE05.8
- •constitutional gigantismE34.4
- •constitutional tall statureE34.4
- •increased secretion from endocrine pancreas of growth hormone-releasing hormoneE16.8
Related Codes(4)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(126)
SNOMED CT
- Eunuchoid gigantism2041006
- Eunuchoidal giant2041006
- Hypersomatotropism3652007
- Overproduction of growth hormone3652007
- Gigantism due to somatostatin deficiency12331003
- Acromegalic arthritis27713005
- Arthropathy associated with acromegaly27713005
- HA - Hyperactivity44548000
- Hyperactive behavior44548000
- Hyperactive behaviour44548000
- Hyperkinesia44548000
- Hyperkinesis44548000
- Increased purposeful goal-directed activity44548000
- Endocrine myopathy57958006
- Muscle disease related to endocrine disease57958006
- Muscle disorders associated with endocrine disease57958006
- Acromegalia74107003
- Acromegaly74107003
- Anterior pituitary adenoma syndrome74107003
- Growth hormone hypersecretion syndrome74107003
- Marie disease74107003
- STH hypersecretion syndrome74107003
- Cerebral giant75968004
- Cerebral gigantism75968004
- Cerebral gigantism syndrome75968004
- Sotos syndrome75968004
- Sotos' syndrome75968004
- Genetic giant80849007
- Giant80849007
- Giantism80849007
- Gigantism80849007
- Normal giant80849007
- Primordial giant80849007
- Acromegalic gigantism86073008
- Hypersomatotropic gigantism86073008
- Launois syndrome86073008
- Pituitary gigantism86073008
- Neuropathy in acromegaly230581008
- Myopathy in acromegaly240089002
- Acromegalic facies248197006
- Large, broad feet249796003
- Acromegaly and gigantism267386008
- Gigantism and acromegaly267386008
- Acromegalic feet275311008
- Hypermelanosis due to endocrine disorder402611000
- Hypermelanosis due to acromegaly403254007
- X-linked intellectual disability with acromegaly and hyperactivity syndrome719826004
- Familial infantile gigantism773645004
- Hereditary infantile gigantism773645004
- Infantile gigantism due to pituitary hyperplasia773645004
- Chromosome Xq26 microduplication syndrome789187001
- X-LAG (X-linked acrogigantism) due to Xq26 microduplication789187001
- X-linked acrogigantism due to Xq26 microduplication789187001
- Acromegalic cardiomyopathy1186866009
- Cardiomyopathy due to acromegaly1186866009
UMLS
- Acromegaly and gigantismC0405578
- Acromegaly and pituitary gigantismC0405578
- Gigantism and acromegalyC0405578
- Gigantism and acromegaly (disorder)C0405578
- acromegaly gigantismC0405578
- gigantism acromegalyC0405578
- gigantism and acromegalyC0405578
- Growth hormone overproductionC0271547
- HypersomatotropismC0271547
- Overproduction of growth hormoneC0271547
- Overproduction of growth hormone (disorder)C0271547
Clinical Terms
- STH hypersecretion syndrome
- Hyperkinesia
- Giant
- Normal giant
- Infantile gigantism due to pituitary hyperplasia
- Cerebral gigantism syndrome
- Pituitary gigantism
- Acromegalic gigantism
- Hyperactive behaviour
- Endocrine myopathy
- Increased purposeful goal-directed activity
- Marie disease
- Cerebral gigantism
- Hyperkinesis
- gigantism acromegaly
- Growth hormone hypersecretion syndrome
- Arthropathy associated with acromegaly
- Muscle disorders associated with endocrine disease
- Hypersomatotropism
- X-linked intellectual disability with acromegaly and hyperactivity syndrome
- Overproduction of growth hormone (disorder)
- Acromegaly
- Hypermelanosis due to acromegaly
- Gigantism and acromegaly
- Hypersomatotropic gigantism
- Hypermelanosis due to endocrine disorder
- Chromosome Xq26 microduplication syndrome
- acromegaly gigantism
- Gigantism due to somatostatin deficiency
- Giantism
- Neuropathy in acromegaly
- Acromegalic feet
- Eunuchoid gigantism
- Muscle disease related to endocrine disease
- Gigantism
- Overproduction of growth hormone
- Hyperactive behavior
- Acromegaly and gigantism
- Eunuchoidal giant
- Acromegalic cardiomyopathy
- Anterior pituitary adenoma syndrome
- Primordial giant
- Familial infantile gigantism
- Growth hormone overproduction
- Acromegalic arthritis
- Sotos syndrome
- X-linked acrogigantism due to Xq26 microduplication
- Hereditary infantile gigantism
- Launois syndrome
- Sotos' syndrome
- Genetic giant
- HA - Hyperactivity
- Myopathy in acromegaly
- Acromegalic facies
- Cardiomyopathy due to acromegaly
- X-LAG (X-linked acrogigantism) due to Xq26 microduplication
- Gigantism and acromegaly (disorder)
- Acromegalia
- Cerebral giant
- Large, broad feet
Frequently Asked Questions
What is the ICD-10 code for acromegaly and pituitary gigantism?
The ICD-10-CM code for acromegaly and pituitary gigantism is E22.0. The full clinical description is "Acromegaly and pituitary gigantism". E22.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E22.0 mean?
ICD-10-CM code E22.0 represents “Acromegaly and pituitary gigantism”. 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 E22.0 a billable code?
Yes, E22.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E22.0 in?
E22.0 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E22.0?
E22.0 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 8 more.
What SNOMED CT codes does E22.0 map to?
E22.0 maps to 22 SNOMED CT concepts: 74107003, 27713005, 1186866009, 248197006, 275311008, and 17 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E22.0?
E22.0 is linked to 2 UMLS Concept Unique Identifiers: C0405578, C0271547. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E22.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like acromegaly and pituitary gigantism 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 E22.0?
E22.0 maps to the ICD-11 code: 5A60.0 (Acromegaly or pituitary gigantism).
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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.