E23.6
BillableOther disorders of pituitary gland
Other disorders of pituitary gland
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Abscess of pituitary
- Adiposogenital dystrophy
Includes
Conditions included under this code
- the listed conditions whether the disorder is in the pituitary or the hypothalamus
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(5)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(296)
SNOMED CT
- Isolated TRH deficiency10736002
- Isolated thyroid hormone releasing hormone deficiency10736002
- Isolated thyroliberin deficiency10736002
- Always thirsty17173007
- Desperate to drink17173007
- Excessive thirst17173007
- Keen for fluids17173007
- Diencephalic syndrome of infancy45740001
- Rathke pouch cyst52859009
- Rathke's cleft cyst52859009
- Rathke's pouch cyst52859009
- Necrosis of pituitary59572000
- Lymphocytic hypophysitis61701006
- Lymphocytic hypopituitarism61701006
- Adiposogenital dystrophy62999006
- Adiposogenital syndrome62999006
- Froehlich syndrome62999006
- Frohlich's syndrome62999006
- Hypothalamic infantilism with obesity syndrome62999006
- Launois-Cleret syndrome62999006
- Disorder of neurohypophysis72442006
- Disorder of neurophysis72442006
- Disorder of posterior pituitary72442006
- Neurohypophysis disorder72442006
- Posterior pituitary disease72442006
- Posterior pituitary disorder72442006
- Hypothalamic obesity82793005
- CSF - Cerebrospinal rhinorrhea85638002
- CSF - Cerebrospinal rhinorrhoea85638002
- Cerebrospinal fluid rhinorrhea85638002
- Cerebrospinal fluid rhinorrhoea85638002
- Cerebrospinal rhinorrhea85638002
- Cerebrospinal rhinorrhoea85638002
- Iatrogenic pituitary disorder86842008
- Pituitary infarct95830009
- Pituitary infarction95830009
- Syndrome of diencephalo-hypophyseal origin111548007
- Abnormality of somatostatin secretion237577005
- Abnormality of neurotensine secretion237595008
- Excessive neurotensine secretion237595008
- Pituitary stalk compression hyperprolactinaemia237664006
- Pituitary stalk compression hyperprolactinemia237664006
- Anterior pituitary hyperplasia237674009
- Somatotroph hyperplasia237675005
- Lactotroph hyperplasia237676006
- Gonadotroph hyperplasia237677002
- Thyrotroph hyperplasia237678007
- Corticotroph hyperplasia237680001
- Oxytocin deficiency237697007
- Pituitary apoplexy237701005
- Pituitary haemorrhage237702003
- Pituitary hemorrhage237702003
- Pituitary fibrosis237703008
- Pituitary fibrosis with midline fibrosis237704002
- Hypophysitis237705001
- Autoimmune hypophysitis237706000
- Lymphocytic hypophysitis of pregnancy237707009
- Granulomatous giant-cell hypophysitis237708004
- Pituitary granuloma237710002
- Pituitary cyst237716008
- Pituitary gland enlarged237718009
- Empty sella syndrome237722004
- Pituitary stalk compression237723009
- Hypothalamic disorder of appetite237724003
- Diencephalic syndrome237733001
- Epidermoid cyst of brain276837006
- Postpartum intrapituitary haemorrhage291665000
- Postpartum intrapituitary hemorrhage291665000
- Endogenous obesity297500005
- Obesity of endocrine origin298464002
- Fetal endocrine disorder363128000
- Foetal endocrine disorder363128000
- Obesity by contributing factors414919008
- Colloid cyst of pituitary gland445158000
- Hypoparathyroidism due to impaired PTH secretion717895004
- Hypoparathyroidism due to impaired parathormone secretion717895004
- Pituitary deficiency due to Rathke cleft cysts783009008
- Pituitary deficiency due to Rathke's cleft cysts783009008
- Infundibulo panhypophysitis783016009
- Panhypophysitis783016009
- Infundibulo neurohypophysitis783158009
- Adenohypophysitis783243008
- Anterior pituitary hypophysitis783243008
- Epidermoid cyst of pituitary1144893005
- Epidermoid cyst of pituitary gland1144893005
- Pituitary epidermoid cyst1144893005
- Immunoglobulin G4 related hypophysitis1186834004
- Xanthogranulomatous hypophysitis1186907003
- Xanthomatous hypophysitis1186907003
- Obesity due to pituitary disease1187531009
- Degeneration of pituitary gland1187547006
- Degeneration of pituitary structure1187547006
- Pituitary degeneration1187547006
- Cyst of craniobuccal pouch1187549009
- Cyst of fetal Rathke pouch1187549009
- Cyst of fetal Rathke's pouch1187549009
- Cyst of foetal Rathke pouch1187549009
- Cyst of foetal Rathke's pouch1187549009
- Hypertrophy of pituitary1187552001
- Hypertrophy of pituitary gland1187552001
- Pituitary hypertrophy1187552001
- Cerebrospinal fluid rhinorrhea due to empty sella syndrome1259111000
- Cerebrospinal fluid rhinorrhoea due to empty sella syndrome1259111000
- Cranial cerebrospinal fluid leak due to empty sella syndrome1259540009
- Leak of cranial cerebrospinal fluid due to empty sella syndrome1259540009
- Cranial cerebrospinal fluid fistula1259545004
- Cranial cerebrospinal fluid leak1259545004
- Leak of cranial cerebrospinal fluid1259545004
- Congenital cyst of brain1363237002
- Congenital cyst of cerebrum1363238007
- Drug induced hypophysitis1365720005
- Drug-induced hypophysitis1365720005
- Hypophysitis caused by drug1365720005
- Inflammation of pituitary caused by drug1365720005
- Colloid brain cyst10481000119108
- Fetal malformation of central nervous system9721000119107
- Foetal malformation of central nervous system9721000119107
- Malformation of central nervous system of fetus9721000119107
- Malformation of central nervous system of foetus9721000119107
- IgG4 related disease10743271000119103
- Immunoglobulin G4 related disease10743271000119103
- Immunoglobulin G4 related systemic disease10743271000119103
- Mass of neurohypophysis541001000124106
- Mass of posterior lobe of pituitary541001000124106
UMLS
- Abscess of pituitaryC0271543
- Abscess of pituitary (disorder)C0271543
- Pituitary AbscessC0271543
- Adiposogenital DystrophyC0016724
- Adiposogenital dystrophyC0016724
- Adiposogenital dystrophy (disorder)C0016724
- Adiposogenital syndromeC0016724
- Babinski-Froelich SyndromeC0016724
- Dystrophia AdiposogenitalisC0016724
- Froehlich SyndromeC0016724
- Froehlich syndromeC0016724
- Froehlich's SyndromeC0016724
- Froehlichs SyndromeC0016724
- Froelich's SyndromeC0016724
- Frohlich SyndromeC0016724
- Frohlich's SyndromeC0016724
- Frohlich's syndromeC0016724
- Frolich's SyndromeC0016724
- Fröhlich SyndromeC0016724
- Hypothalamic Infantilism-ObesityC0016724
- Hypothalamic infantilism with obesity syndromeC0016724
- Launois-Cleret SyndromeC0016724
- Launois-Cleret syndromeC0016724
- Sexual InfantilismC0016724
- Syndrome, Froehlich'sC0016724
- adiposogenital dystrophyC0016724
- adiposogenital syndromeC0016724
- froehlich syndromeC0016724
- frohlich syndromeC0016724
- frohlich's syndromeC0016724
- frohlichs syndromeC0016724
- Other disorders of pituitary glandC0348457
Clinical Terms
- Drug-induced hypophysitis
- Pituitary stalk compression hyperprolactinaemia
- Adenohypophysitis
- Hypertrophy of pituitary
- Necrosis of pituitary
- Congenital cyst of cerebrum
- CSF - Cerebrospinal rhinorrhoea
- Panhypophysitis
- Pituitary stalk compression hyperprolactinemia
- Pituitary hypertrophy
- Posterior pituitary disease
- Abscess of pituitary
- Fröhlich Syndrome
- Cyst of foetal Rathke's pouch
- Isolated thyroid hormone releasing hormone deficiency
- Obesity due to pituitary disease
- Hypophysitis caused by drug
- frohlich's syndrome
- Isolated thyroliberin deficiency
- Colloid cyst of pituitary gland
- Iatrogenic pituitary disorder
- Anterior pituitary hyperplasia
- Froehlich's Syndrome
- Always thirsty
- Adiposogenital syndrome
- Diencephalic syndrome
- Mass of posterior lobe of pituitary
- Pituitary Abscess
- Infundibulo neurohypophysitis
- Foetal endocrine disorder
- Pituitary epidermoid cyst
- Abscess of pituitary (disorder)
- Fetal endocrine disorder
- Leak of cranial cerebrospinal fluid due to empty sella syndrome
- Hypertrophy of pituitary gland
- Pituitary gland enlarged
- Abnormality of neurotensine secretion
- Lymphocytic hypophysitis of pregnancy
- Dystrophia Adiposogenitalis
- Pituitary fibrosis with midline fibrosis
- CSF - Cerebrospinal rhinorrhea
- Hypothalamic Infantilism-Obesity
- Cyst of foetal Rathke pouch
- Empty sella syndrome
- Mass of neurohypophysis
- Neurohypophysis disorder
- Babinski-Froelich Syndrome
- Rathke's pouch cyst
- Froehlich Syndrome
- Adiposogenital Dystrophy
- Cyst of craniobuccal pouch
- Granulomatous giant-cell hypophysitis
- Degeneration of pituitary structure
- Endogenous obesity
- Anterior pituitary hypophysitis
- Pituitary apoplexy
- Pituitary hemorrhage
- Drug induced hypophysitis
- Frolich's Syndrome
- Xanthomatous hypophysitis
- frohlichs syndrome
- Pituitary infarct
- Epidermoid cyst of pituitary gland
- Excessive thirst
- Hypothalamic infantilism with obesity syndrome
- Inflammation of pituitary caused by drug
- Lymphocytic hypophysitis
- Xanthogranulomatous hypophysitis
- Rathke's cleft cyst
- Corticotroph hyperplasia
- Hypophysitis
- Cyst of fetal Rathke's pouch
- Cyst of fetal Rathke pouch
- Pituitary fibrosis
- Obesity by contributing factors
- Pituitary deficiency due to Rathke cleft cysts
- Lymphocytic hypopituitarism
- frohlich syndrome
- Syndrome, Froehlich's
- Cranial cerebrospinal fluid fistula
- Cerebrospinal fluid rhinorrhea due to empty sella syndrome
- Immunoglobulin G4 related hypophysitis
- Cerebrospinal fluid rhinorrhoea
- Gonadotroph hyperplasia
- Cerebrospinal rhinorrhea
- Malformation of central nervous system of fetus
- IgG4 related disease
- Thyrotroph hyperplasia
- Pituitary haemorrhage
- Launois-Cleret syndrome
- Postpartum intrapituitary hemorrhage
- Cerebrospinal fluid rhinorrhoea due to empty sella syndrome
- Hypothalamic disorder of appetite
- Excessive neurotensine secretion
- Autoimmune hypophysitis
- Desperate to drink
- Epidermoid cyst of pituitary
- Cranial cerebrospinal fluid leak due to empty sella syndrome
- Infundibulo panhypophysitis
- Obesity of endocrine origin
- Posterior pituitary disorder
- Abnormality of somatostatin secretion
- Postpartum intrapituitary haemorrhage
- Keen for fluids
- Cerebrospinal rhinorrhoea
- Malformation of central nervous system of foetus
- Epidermoid cyst of brain
- Isolated TRH deficiency
- Cerebrospinal fluid rhinorrhea
- Syndrome of diencephalo-hypophyseal origin
- Pituitary deficiency due to Rathke's cleft cysts
- Adiposogenital dystrophy (disorder)
- Cranial cerebrospinal fluid leak
- Pituitary cyst
- Froelich's Syndrome
- Hypothalamic obesity
- Disorder of posterior pituitary
- Pituitary granuloma
- Foetal malformation of central nervous system
- Degeneration of pituitary gland
- Pituitary degeneration
- Sexual Infantilism
- Somatotroph hyperplasia
- Froehlichs Syndrome
- Disorder of neurohypophysis
- Immunoglobulin G4 related systemic disease
- Colloid brain cyst
- Hypoparathyroidism due to impaired PTH secretion
- Rathke pouch cyst
- Diencephalic syndrome of infancy
- Fetal malformation of central nervous system
- Disorder of neurophysis
- Hypoparathyroidism due to impaired parathormone secretion
- Pituitary stalk compression
- Pituitary infarction
- Oxytocin deficiency
- Congenital cyst of brain
- Lactotroph hyperplasia
- Leak of cranial cerebrospinal fluid
- Immunoglobulin G4 related disease
Frequently Asked Questions
What is the ICD-10 code for other disorders of pituitary gland?
The ICD-10-CM code for other disorders of pituitary gland is E23.6. The full clinical description is "Other disorders of pituitary gland". E23.6 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E23.6 mean?
ICD-10-CM code E23.6 represents “Other disorders of pituitary gland”. 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 E23.6 a billable code?
Yes, E23.6 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E23.6 in?
E23.6 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E23.6?
E23.6 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 E23.6 map to?
E23.6 maps to 67 SNOMED CT concepts: 237595008, 237577005, 783243008, 62999006, 17173007, and 62 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E23.6?
E23.6 is linked to 3 UMLS Concept Unique Identifiers: C0271543, C0016724, C0348457. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E23.6 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of pituitary gland 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 E23.6?
E23.6 maps to the ICD-11 code: 5A6Z (Disorders of the pituitary hormone system, unspecified).
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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.