E23.0
BillableHypopituitarism
Hypopituitarism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Fertile eunuch syndrome
- Hypogonadotropic hypogonadism
- Idiopathic growth hormone deficiency
- Isolated deficiency of gonadotropin
- Isolated deficiency of growth hormone
- Isolated deficiency of pituitary hormone
- Kallmann's syndrome
- Lorain-Levi short stature
- Necrosis of pituitary gland (postpartum)
- Panhypopituitarism
- Pituitary cachexia
- Pituitary insufficiency NOS
- Pituitary short stature
- Sheehan's syndrome
- Simmonds' disease
Includes
Conditions included under this code
- the listed conditions whether the disorder is in the pituitary or the hypothalamus
Also Known As / Clinical Terms
SNOMED CT
- Secondary hypopituitarism442001
- IGHD - Isolated growth hormone deficiency2109003
- Isolated growth hormone deficiency2109003
- Isolated growth hormone insufficiency2109003
- Isolated somatotropin deficiency2109003
- Asexual dwarfism7530009
- Brissaud dwarfism7530009
- Brissaud-Meige syndrome7530009
- Burnier syndrome7530009
- Frohlich dwarfism7530009
- Hypophyseal infantilism7530009
- Hypopituitary dwarfism with failure of development of sexual characteristics7530009
- Lorain-Levi dwarfism7530009
- Nebecourt syndrome7530009
- Fleischer syndrome7990002
- Growth hormone deficiency with hypogammaglobulinaemia7990002
- Growth hormone deficiency with hypogammaglobulinemia7990002
- Immunoglobulinaemia with isolated somatotropin deficiency7990002
- Immunoglobulinemia with isolated somatotropin deficiency7990002
- Fertile eunuch8829008
- Fertile eunuch syndrome8829008
- Isolated lutropin deficiency8829008
- Isolated gonadotrophin deficiency10340008
- Isolated gonadotropin deficiency10340008
- Hereditary sensory neuropathy11442006
- Posterior sensory radicular neuropathy11442006
- Myopathy in hypopituitarism14289006
- Autosomal recessive isolated somatotropin deficiency18200000
- Isolated growth hormone deficiency type I18200000
- Pituitary dwarfism type I18200000
- Nonfamilial asexual dwarfism20900005
- Transient somatotropin deficiency22306000
- Central hypothyroidism26692000
- Familial enlargement of the sella turcica27270004
- Pituitary dwarfism with large sella turcica27270004
- Anaemia of endocrine disorder31820007
- Anemia of endocrine disorder31820007
- Deficient secretion of all pituitary hormones32390006
- Panhypopituitarism32390006
- Primary hypopituitarism32390006
- Simmond's disease32390006
- Simmonds' disease32390006
- Gonadotrophin deficiency33927004
- Hypogonadotropic hypogonadism33927004
- Secondary hypogonadism33927004
- Ateliotic dwarfism with hyperinsulinaemia38576000
- Ateliotic dwarfism with hyperinsulinemia38576000
- Nonfamilial hyperinsulinaemic isolated somatotropin deficiency38576000
- Nonfamilial hyperinsulinemic isolated somatotropin deficiency38576000
- Hypopituitarism due to pituitary neoplasm40781006
- Hypopituitarism due to pituitary tumor40781006
- Hypopituitarism due to pituitary tumour40781006
- Absent smell44169009
- Anosmia44169009
- Anosmia (loss of sense of smell)44169009
- Loss of sense of smell44169009
- Loss of the sense of smell44169009
- No sense of smell44169009
- Sense of smell absent44169009
- Sense of smell lost44169009
- Pituitary dwarfism with normal somatotropin level AND low somatomedin51371005
- Endocrine myopathy57958006
- Muscle disease related to endocrine disease57958006
- Muscle disorders associated with endocrine disease57958006
- Necrosis of pituitary59572000
- Anaemia of pituitary deficiency60138009
- Anemia of pituitary deficiency60138009
- Axonal neuropathy60703000
- Lymphocytic hypophysitis61701006
- Lymphocytic hypopituitarism61701006
- Hypoprolactinaemia67873006
- Hypoprolactinemia67873006
- Isolated prolactin deficiency67873006
- Prolactin deficiency67873006
- Moyamoya disease69116000
- Ateleiotic dwarfism71003000
- Ateliotic dwarfism71003000
- Hypopituitary dwarfism with normal sexual characteristics71003000
- Idiopathic pituitary dwarfism71003000
- Sexual ateleiotic dwarfism71003000
- Sexual ateliotic dwarfism71003000
- Sexual dwarfism71003000
- Deficient secretion of one OR more pituitary hormones74728003
- Hypopituitarism74728003
- Pituitary deficiency74728003
- Pituitary failure74728003
- Pituitary hypofunction74728003
- Pituitary insufficiency74728003
- Hypoplasia of eye86527000
- Rudimentary eye86527000
- Pituitary cachexia89476005
- Abnormal sella turcica syndrome91187007
- Familial absence of sella turcica91187007
- Familial panhypopituitarism with abnormal sella turcica91187007
- Ferrier-Stone syndrome91187007
- Pituitary dwarfism with small sella turcica91187007
- Primary empty sella syndrome91187007
- Congenital hypoplasia of nose93278002
- Congenital hypoplastic nose93278002
- Congenital small nose93278002
- Congenital stenosis of carotid artery93396008
- Anosmia eunuchoidism93559003
- Dysplasia olfactogenitalis of de Morsier93559003
- Gonadotrophin deficiency with anosmia93559003
- Hypogonadism with anosmia93559003
- Kallman syndrome93559003
- Kallman's syndrome93559003
- Kallmann's syndrome93559003
- Olfactogenital dysplasia93559003
- Sensory neuropathy95662005
- Prepuberal panhypopituitarism123760002
- Idiopathic gonadotrophin deficiency123953004
- Idiopathic hypogonadotropic hypogonadism123953004
- Peripheral axonal neuropathy128208007
- Ateliotic dwarfism without insulinopenia178456000
- Idiopathic panhypopituitarism190470005
- Post-infarction panhypopituitarism190472002
- Follicle stimulating hormone deficiency190480009
- LH - luteinising hormone deficiency190481008
- LH - luteinizing hormone deficiency190481008
- Luteinizing hormone deficiency190481008
- Female infertility of pituitary - hypothalamic origin198448006
- Primary pituitary - hypothalamic infertility198449003
- Secondary pituitary - hypothalamic infertility198450003
- Congenital disorder of facial nerve230541001
- Congenital facial nerve palsy230542008
- ICA - Internal carotid artery stenosis233964008
- Internal carotid artery stenosis233964008
- Immunodeficiency with major anomalies234631003
- Immunodeficiency associated with multiple organ system abnormalities234641000
- Panhypopituitarism - anterior and posterior237682009
- Panhypopituitarism - X-linked237683004
- X-linked panhypopituitarism237683004
- Postpartum pituitary necrosis237684005
- Sheehan syndrome237684005
- Sheehan's syndrome237684005
- Partial hypopituitarism237685006
- Autosomal dominant isolated somatotropin deficiency237687003
- Isolated growth hormone deficiency - autosomal dominant237687003
- IGHD - Idiopathic growth hormone deficiency237688008
- Idiopathic growth hormone deficiency237688008
- Idiopathic growth hormone insufficiency237688008
- Growth hormone neurosecretory dysfunction237689000
- Psychosocial growth hormone deficiency237691008
- Psychosocial growth hormone insufficiency237691008
- ACTH deficiency237692001
- Adrenocorticotropic hormone (ACTH) deficiency237692001
- Adrenocorticotropic hormone deficiency237692001
- Secondary hypoadrenalism237692001
- Hypopituitarism secondary to head trauma237699005
- Post-traumatic hypopituitarism237699005
- Morbid obesity238136002
- Partial loss of hair247541001
- Congenital anomaly of anterior pituitary254255007
- Congenital malformation of anterior pituitary254255007
- Idiopathic hypopituitarism267388009
- Post-birth injury hypopituitarism267389001
- Post-infarction hypopituitarism267390005
- Post-infective hypopituitarism271386001
- Post-infective panhypopituitarism271386001
- Postpartum hypopituitarism290653008
- Female hypogonadotropic hypogonadism361117008
- Sequelae of endocrine disorders363297005
- Hypopituitary dwarfism367460001
- Hyposomatotropic dwarfism367460001
- Isolated deficiency of growth hormone in children367460001
- Lorain - Levi dwarfism367460001
- Pituitary dwarfism367460001
- Pituitary nanism367460001
- Prepuberal dwarfism367460001
- Prepubertal dwarfism367460001
- Primary failure of the testes370997001
- Primary testicular failure370997001
- GHD - Growth hormone deficiency397827003
- Growth hormone deficiency397827003
- Growth hormone insufficiency397827003
- Adult-onset growth hormone deficiency420351005
- Hypogonadotropic hypogonadism due to isolated gonadotrophin deficiency420499009
- Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency420499009
- Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency421019006
- Adult growth hormone deficiency421684006
- Hypogonadotropic hypogonadism due to luteinising hormone deficiency421821002
- Hypogonadotropic hypogonadism due to luteinizing hormone deficiency421821002
- Adult growth hormone deficiency with onset in childhood421931005
- Deficiency of gonadotrophin releasing factor422240004
- Deficiency of gonadotropin releasing factor422240004
- Gonadotrophin releasing factor deficiency422240004
- Gonadotrophin releasing hormone deficiency422240004
- Gonadotropin releasing factor deficiency422240004
- Gonadotropin releasing hormone deficiency422240004
- Luteinising hormone-releasing hormone deficiency422240004
- Luteinizing hormone-releasing hormone deficiency422240004
- Growth hormone deficiency after bone marrow transplant429514007
- Obesity, early-onset, adrenal insufficiency, and red hair702949005
- Proopiomelanocortin deficiency syndrome702949005
- Hypopituitarism due to empty sella turcica syndrome715668008
- Pituitary deficiency due to empty sella turcica syndrome715668008
- Combined pituitary hormone deficiency genetic form718182008
- Familial congenital hypopituitarism718182008
- Multiple pituitary hormone deficiency genetic form718182008
- Al Awadi Farag Teebi syndrome719275009
- Primary hypergonadotropic hypogonadism and partial alopecia syndrome719275009
- Cardiogenital syndrome719451006
- Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome719451006
- Malouf syndrome719451006
- Najjar syndrome719451006
- Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome720981000
- Devriendt Vandenberghe Fryns syndrome720981000
- Cataract and testicular failure syndrome721233005
- Hypergonadotropic hypogonadism with cataract syndrome721233005
- Lubinsky syndrome721233005
- Hypopituitarism following procedure721288009
- Postprocedural hypopituitarism721288009
- Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome721842008
- Salti Salem syndrome721842008
- Kallman syndrome with cardiopathy722027009
- Kallman syndrome with heart disease722027009
- Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome722380003
- Martsolf syndrome722380003
- Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome722459008
- Sohval Soffer syndrome722459008
- Acquired central hypothyroidism722940002
- Congenital hypogonadotropic hypogonadism722944006
- RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia) syndrome723999009
- RHYNS syndrome723999009
- Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome723999009
- Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome724097003
- Moyamoya disease, short stature, facial dysmorphism, hypergonadotropic hypogonadism724097003
- Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome724174003
- Bosma Henkin Christiansen syndrome724281002
- Bosma arhinia microphthalmia syndrome724281002
- Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome724281002
- Microcephalus, hypergonadotropic hypogonadism, short stature syndrome733092009
- Mikati Najjar Sahli syndrome733092009
- Chang Davidson Carlson syndrome733113002
- Hypogonadotropic hypogonadism retinitis pigmentosa syndrome733113002
- Isolated FSH (follicle stimulating hormone) deficiency758664007
- Isolated follicle stimulating hormone deficiency758664007
- Non-acquired combined pituitary hormone deficiency, deafness, rigid cervical spine syndrome771308008
- Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome771308008
- RAB18 deficiency772225005
- RAB18, member RAS oncogene family deficiency772225005
- DAVID (deficiency in anterior pituitary function, variable immunodeficiency) syndrome773664005
- Deficiency in anterior pituitary function, variable immunodeficiency syndrome773664005
- Hypogonadotropic hypogonadism, severe microcephaly, sensorineural deafness, dysmorphism syndrome773665006
- Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome773665006
- Late-onset isolated ACTH (adrenocorticotropic hormone) deficiency773989002
- Late-onset isolated ACTH deficiency773989002
- Late-onset isolated adrenocorticotropic hormone deficiency773989002
- Functional hypogonadotropic hypogonadism846680003
- Amenorrhea due to Kallman syndrome1144947008
- Amenorrhea due to congenital GnRH (gonadotrophin releasing hormone) deficiency1144947008
- Amenorrhea due to congenital gonadotrophin releasing hormone deficiency1144947008
- Amenorrhoea due to Kallman syndrome1144947008
- Amenorrhoea due to congenital GnRH (gonadotrophin releasing hormone) deficiency1144947008
- Amenorrhoea due to congenital gonadotrophin releasing hormone deficiency1144947008
- Acquired central hypothyroidism due to Sheehan syndrome1179381000
- Acquired central hypothyroidism due to disorder of pituitary gland1179382007
- Acquired central hypothyroidism due to pituitary disorder1179382007
- Hereditary growth hormone deficiency1186807002
- Hypopituitarism due to disorder of blood vessel1186833005
- Hypopituitarism due to vascular disorder1186833005
- Hypopituitarism due to disorder characterised by granuloma1186835003
- Hypopituitarism due to disorder characterized by granuloma1186835003
- Hypopituitarism due to granulomatous disease1186835003
- Hypopituitarism due to metabolic disease1186837006
- Autoimmune hypopituitarism1186855002
- Avascular necrosis of pituitary gland1217046003
- Ischaemic pituitary necrosis1217046003
- Ischemic pituitary necrosis1217046003
- Isolated deficiency of pituitary hormone1217051009
- Isolated pituitary hormone deficiency1217051009
- CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome1220595008
- Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome1220595008
- Body height below reference range1363478003
- Anterior pituitary hormone deficiency2851000119101
- Intracranial carotid artery stenosis450440061000119108
- Stenosis of intracranial carotid artery450440061000119108
- Partial growth hormone deficiency17151000119108
- Short stature co-occurrent and due to endocrine disorder368331000119100
UMLS
- HypopituitalismC0020635
- HypopituitarismC0020635
- ADENOHYPOPHYSEAL HYPOSECRETC0020635
- ANTERIOR PITUITARY HYPOSECRET SYNDROMEC0020635
- Adenohypophyseal HyposecretionC0020635
- Anterior Pituitary Hyposecretion SyndromeC0020635
- Deficient secretion of one OR more pituitary hormonesC0020635
- HYPOSECRET ADENOHYPOPHYSEALC0020635
- HYPOSECRET SYNDROME ANTERIOR PITUITARYC0020635
- Hypopituitarism (disorder)C0020635
- Hyposecretion Syndrome, Anterior PituitaryC0020635
- Hyposecretion, AdenohypophysealC0020635
- Insufficiency pituitaryC0020635
- Insufficiency, PituitaryC0020635
- Pituitary InsufficiencyC0020635
- Pituitary deficiencyC0020635
- Pituitary failureC0020635
- Pituitary hypofunctionC0020635
- Pituitary insufficiencyC0020635
- Pituitary insufficiency NOSC0020635
- deficiencies pituitaryC0020635
- hypopituitarismC0020635
- insufficiency pituitaryC0020635
- pituitary failureC0020635
- pituitary hypofunctionC0020635
- pituitary insufficiencyC0020635
- ANOSMIC HYPOGONADISMC0162809
- Anosmia eunuchoidismC0162809
- Anosmic HypogonadismC0162809
- Anosmic HypogonadismsC0162809
- Anosmic Idiopathic Hypogonadotropic HypogonadismC0162809
- Anosmic hypogonadismC0162809
- Anosmic idiopathic hypogonadotropic hypogonadismC0162809
- DYSPLASIA OLFACTOGENITALIS OF DE MORSIERC0162809
- Dysplasia Olfactogenitalis of De MorsierC0162809
- Dysplasia olfactogenitalis of de MorsierC0162809
- Gonadotrophin deficiency with anosmiaC0162809
- HHAC0162809
- HYPOGONADOTROPIC HYPOGONADISM AND ANOSMIAC0162809
- Hypogonadism with anosmiaC0162809
- Hypogonadism with anosmia (disorder)C0162809
- Hypogonadism, AnosmicC0162809
- Hypogonadisms, AnosmicC0162809
- Hypogonadotropic Hypogonadism and AnosmiaC0162809
- Hypogonadotropic Hypogonadism with AnosmiaC0162809
- Hypogonadotropic Hypogonadism-Anosmia SyndromeC0162809
- Hypogonadotropic hypogonadism and anosmiaC0162809
- Hypogonadotropic hypogonadism-anosmia syndromeC0162809
- Kallman syndromeC0162809
- Kallman's syndromeC0162809
- Kallmann SyndromeC0162809
- Kallmann syndromeC0162809
- Kallmann's SyndromeC0162809
- Kallmann's syndromeC0162809
- Kallmanns SyndromeC0162809
- Olfacto genital dysplasiaC0162809
- Olfactogenital dysplasiaC0162809
- Syndrome, KallmannC0162809
- Syndrome, Kallmann'sC0162809
- de Morsier-Kallman's syndromeC0162809
- de morsier syndromeC0162809
- familial hypogonadism with anosmiaC0162809
- kallman syndromeC0162809
- kallman's syndromeC0162809
- kallmann syndromeC0162809
- kallmann's syndromeC0162809
- kallmanns syndromeC0162809
- kallmans syndromeC0162809
- CPHDC0242343
- Combined Pituitary Hormone DeficiencyC0242343
- Combined pituitary hormone deficiencyC0242343
- Complete HypopituitarismC0242343
- Deficient secretion of all pituitary hormonesC0242343
- PANHYPOPITUITARISMC0242343
- PanhypopituitarismC0242343
- Panhypopituitarism (disorder)C0242343
- Primary hypopituitarismC0242343
- panhypopituitarismC0242343
- primary hypopituitarismC0242343
- Central HypogonadismC0271623
- Gonadotrophin deficiencyC0271623
- Hypogonadism, HypogonadotropicC0271623
- Hypogonadism, hypogonadotropicC0271623
- Hypogonadotrophic hypogonadismC0271623
- Hypogonadotropic HypogonadismC0271623
- Hypogonadotropic hypogonadismC0271623
- Hypogonadotropic hypogonadism (disorder)C0271623
- Low gonadotropins (secondary hypogonadism)C0271623
- Secondary HypogonadismC0271623
- Secondary hypogonadismC0271623
- hypogonadotrophic hypogonadismC0271623
- hypogonadotropic hypogonadismC0271623
- secondary hypogonadismC0271623
- DWARFISM GROWTH HORMONE DEFICC0013338
- Dwarfism, Growth Hormone DeficiencyC0013338
- Dwarfism, PituitaryC0013338
- Dwarfism, growth hormone deficiencyC0013338
- Dwarfism, pituitaryC0013338
- GROWTH HORMONE DEFIC DWARFISMC0013338
- Growth Hormone Deficiency DwarfismC0013338
- Growth hormone deficiency dwarfismC0013338
- Hypopituitary dwarfismC0013338
- Hyposomatotrophic DwarfismC0013338
- Hyposomatotropic dwarfismC0013338
- Isolated GH DeficiencyC0013338
- Isolated Growth Hormone DeficiencyC0013338
- Isolated HGH DeficiencyC0013338
- Isolated Human Growth Hormone DeficiencyC0013338
- Isolated Somatotropin DeficiencyC0013338
- Isolated Somatotropin Deficiency DisorderC0013338
- Isolated deficiency of growth hormoneC0013338
- Isolated deficiency of growth hormone in childrenC0013338
- Isolated growth hormone deficiencyC0013338
- Isolated somatotropin deficiency disorderC0013338
- Lorain - Levi dwarfismC0013338
- Lorain-Levi dwarfismC0013338
- Lorain-Levi short statureC0013338
- Nanism, PituitaryC0013338
- Pituitary DwarfismC0013338
- Pituitary NanismC0013338
- Pituitary dwarfismC0013338
- Pituitary dwarfism (disorder)C0013338
- Pituitary nanismC0013338
- Prepuberal dwarfismC0013338
- Prepubertal dwarfismC0013338
- dwarfism pituitaryC0013338
- dwarfs pituitaryC0013338
- hypophyseal dwarfC0013338
- hypopituitary dwarfismC0013338
- pituitary dwarfC0013338
- pituitary dwarfismC0013338
- Disease, SimmondsC0242342
- Hypopituitarism, PostpartumC0242342
- Panhypopituitarism, PostpartumC0242342
- Pituitary Insufficiency, PostpartumC0242342
- Postpartum HypopituitarismC0242342
- Postpartum PanhypopituitarismC0242342
- Postpartum Pituitary InsufficiencyC0242342
- Postpartum hypopituitarismC0242342
- Postpartum hypopituitarism (disorder)C0242342
- Postpartum pituitary necrosisC0242342
- SIMMONDS DISC0242342
- Sheehan SyndromeC0242342
- Sheehan syndromeC0242342
- Sheehan's SyndromeC0242342
- Sheehan's syndromeC0242342
- Sheehan's syndrome (disorder)C0242342
- Sheehans SyndromeC0242342
- Simmond's DiseaseC0242342
- Simmond's diseaseC0242342
- Simmonds DiseaseC0242342
- Simmonds' DiseaseC0242342
- Simmonds' diseaseC0242342
- Syndrome, SheehanC0242342
- Syndrome, Sheehan'sC0242342
- postpartum hypopituitarismC0242342
- postpartum pituitary necrosisC0242342
- sheehan syndromeC0242342
- sheehan's syndromeC0242342
- sheehans syndromeC0242342
- sheehans's syndromeC0242342
- simmond's diseaseC0242342
- simmonds diseaseC0242342
- simmonds' diseaseC0242342
- FERTILE EUNUCH SYNDROMEC0271582
- Fertile eunuchC0271582
- Fertile eunuch syndromeC0271582
- HH23C0271582
- HYPOGONADOTROPIC HYPOGONADISM 23 WITH OR WITHOUT ANOSMIAC0271582
- HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIAC0271582
- Isolated lutropin deficiencyC0271582
- Isolated lutropin deficiency (disorder)C0271582
- PASQUALINI SYNDROMEC0271582
- IGHD - Idiopathic growth hormone deficiencyC0342381
- Idiopathic growth hormone deficiencyC0342381
- Idiopathic growth hormone deficiency (disorder)C0342381
- Idiopathic growth hormone insufficiencyC0342381
- Isolated deficiency of gonadotropinC0271577
- Isolated gonadotrophin deficiencyC0271577
- Isolated gonadotropin deficiencyC0271577
- Isolated gonadotropin deficiency (disorder)C0271577
- Isolated deficiency of pituitary hormoneC2874188
- Isolated deficiency of pituitary hormone (disorder)C2874188
- Isolated pituitary hormone deficiencyC2874188
- Necrosis of pituitary gland (postpartum)C2874189
- Pituitary cachexiaC0221405
- Pituitary cachexia (disorder)C0221405
- Pituitary short statureC2874190
Frequently Asked Questions
What is the ICD-10 code for hypopituitarism?
The ICD-10-CM code for hypopituitarism is E23.0. The full clinical description is "Hypopituitarism". E23.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E23.0 mean?
ICD-10-CM code E23.0 represents "Hypopituitarism". 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 E23.0 a billable code?
Yes, E23.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E23.0 in?
E23.0 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E23.0?
E23.0 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 2 more.
What SNOMED CT codes does E23.0 map to?
E23.0 maps to 126 SNOMED CT concepts: 237692001, 91187007, 44169009, 722940002, 1179381000, and 121 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E23.0?
E23.0 is linked to 13 UMLS Concept Unique Identifiers: C0020635, C0162809, C0242343, C0271623, C0013338, and 8 more. 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.