E23.0

Q: What is the ICD-11 equivalent of E23.0?

E23.0 maps to the ICD-11 code: 5A61.0 (Hypopituitarism). This is an equivalent mapping.

Billable

Hypopituitarism

Status

Billable / Specific

Chapter

4: Endocrine, Nutritional and Metabolic Diseases

Block

E20-E35

Parent Code

E23

ICD-11 Mapping

1 equivalent

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

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Related Codes(5)

E23.1

Drug-induced hypopituitarism

Billable E23.2

Diabetes insipidus

Billable E23.3

Hypothalamic dysfunction, not elsewhere classified

Billable E23.6

Other disorders of pituitary gland

Billable E23.7

Disorder of pituitary gland, unspecified

Billable

ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

5A61.0HypopituitarismequivalentPrimary

Also Known As / Clinical Terms(833)

SNOMED CT

UMLS

Clinical Terms

Postpartum Pituitary Insufficiency
Idiopathic panhypopituitarism
Nonfamilial asexual dwarfism
Female hypogonadotropic hypogonadism
Gonadotrophin releasing hormone deficiency
Cardiogenital syndrome
Peripheral axonal neuropathy
Hypogonadotropic hypogonadism
Hypophyseal infantilism
Anosmic idiopathic hypogonadotropic hypogonadism
Brissaud dwarfism
Adrenocorticotropic hormone deficiency
Anaemia of pituitary deficiency
Sohval Soffer syndrome
Sensory neuropathy
RAB18, member RAS oncogene family deficiency
Idiopathic growth hormone insufficiency
Sexual dwarfism
Hyposecretion, Adenohypophyseal
Postpartum pituitary necrosis
Hypopituitary dwarfism with normal sexual characteristics
Simmonds' disease
Acquired central hypothyroidism
Asexual dwarfism
Ateliotic dwarfism with hyperinsulinemia
Partial growth hormone deficiency
Post-birth injury hypopituitarism
Isolated gonadotropin deficiency (disorder)
Luteinizing hormone-releasing hormone deficiency
CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
Isolated Growth Hormone Deficiency
Syndrome, Sheehan's
Disease, Simmonds
Growth hormone deficiency with hypogammaglobulinemia
DWARFISM GROWTH HORMONE DEFIC
Ischaemic pituitary necrosis
Hypoprolactinemia
Isolated deficiency of pituitary hormone
Panhypopituitarism (disorder)
Chang Davidson Carlson syndrome
Adult growth hormone deficiency
Ateliotic dwarfism
Partial loss of hair
Brissaud-Meige syndrome
Post-traumatic hypopituitarism
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural deafness, dysmorphism syndrome
Sense of smell lost
Post-infarction panhypopituitarism
Isolated FSH (follicle stimulating hormone) deficiency
Nonfamilial hyperinsulinemic isolated somatotropin deficiency
Adult-onset growth hormone deficiency
Psychosocial growth hormone deficiency
Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome
Idiopathic growth hormone deficiency (disorder)
Adrenocorticotropic hormone (ACTH) deficiency
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
Panhypopituitarism - X-linked
Combined pituitary hormone deficiency
Ateliotic dwarfism with hyperinsulinaemia
Hereditary sensory neuropathy
CPHD
Hypopituitarism due to pituitary tumour
Lymphocytic hypopituitarism
Pituitary Dwarfism
panhypopituitarism
simmonds disease
Syndrome, Sheehan
Late-onset isolated ACTH (adrenocorticotropic hormone) deficiency
Hypogonadotropic hypogonadism (disorder)
Posterior sensory radicular neuropathy
Isolated deficiency of gonadotropin
Panhypopituitarism, Postpartum
Myopathy in hypopituitarism
Anemia of endocrine disorder
DAVID (deficiency in anterior pituitary function, variable immunodeficiency) syndrome
Pituitary insufficiency NOS
Nonfamilial hyperinsulinaemic isolated somatotropin deficiency
Partial hypopituitarism
Amenorrhea due to congenital gonadotrophin releasing hormone deficiency
FERTILE EUNUCH SYNDROME
dwarfs pituitary
Isolated somatotropin deficiency
Central Hypogonadism
Simmond's Disease
Proopiomelanocortin deficiency syndrome
Isolated Somatotropin Deficiency Disorder
Pituitary dwarfism with normal somatotropin level AND low somatomedin
Dwarfism, Growth Hormone Deficiency
Pituitary failure
Anosmia eunuchoidism
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
Insufficiency pituitary
Muscle disease related to endocrine disease
Luteinizing hormone deficiency
sheehans's syndrome
ADENOHYPOPHYSEAL HYPOSECRET
de Morsier-Kallman's syndrome
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
Adenohypophyseal Hyposecretion
Martsolf syndrome
ICA - Internal carotid artery stenosis
Axonal neuropathy
Luteinising hormone-releasing hormone deficiency
Hypopituitary dwarfism with failure of development of sexual characteristics
ACTH deficiency
Postpartum Panhypopituitarism
HYPOSECRET ADENOHYPOPHYSEAL
Isolated deficiency of growth hormone in children
RAB18 deficiency
Necrosis of pituitary gland (postpartum)
Syndrome, Kallmann's
Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome
Secondary hypoadrenalism
X-linked panhypopituitarism
dwarfism pituitary
Anosmic Hypogonadisms
Idiopathic gonadotrophin deficiency
Amenorrhoea due to congenital GnRH (gonadotrophin releasing hormone) deficiency
Growth hormone deficiency dwarfism
kallmans syndrome
Postprocedural hypopituitarism
kallman syndrome
Hypopituitarism, Postpartum
DYSPLASIA OLFACTOGENITALIS OF DE MORSIER
sheehan syndrome
Najjar syndrome
Isolated growth hormone insufficiency
Isolated growth hormone deficiency type I
Congenital hypogonadotropic hypogonadism
Familial absence of sella turcica
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome
Growth hormone deficiency after bone marrow transplant
Acquired central hypothyroidism due to Sheehan syndrome
Hypopituitalism
Morbid obesity
Salti Salem syndrome
Syndrome, Kallmann
Immunoglobulinaemia with isolated somatotropin deficiency
Follicle stimulating hormone deficiency
Lorain-Levi short stature
Fertile eunuch
Pituitary dwarfism with small sella turcica
Gonadotrophin deficiency with anosmia
Low gonadotropins (secondary hypogonadism)
Stenosis of intracranial carotid artery
Anosmia (loss of sense of smell)
Anterior Pituitary Hyposecretion Syndrome
secondary hypogonadism
kallmanns syndrome
IGHD - Isolated growth hormone deficiency
Hypogonadism, Anosmic
RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia) syndrome
Lymphocytic hypophysitis
Amenorrhea due to Kallman syndrome
Sexual ateliotic dwarfism
Intracranial carotid artery stenosis
Fleischer syndrome
Endocrine myopathy
HHA
Congenital hypoplastic nose
Body height below reference range
Pituitary insufficiency
LH - luteinising hormone deficiency
Anosmic Hypogonadism
Pituitary Insufficiency, Postpartum
Al Awadi Farag Teebi syndrome
Isolated pituitary hormone deficiency
Burnier syndrome
Hypogonadotropic hypogonadism due to isolated gonadotrophin deficiency
PASQUALINI SYNDROME
Hypopituitarism due to pituitary neoplasm
Postpartum hypopituitarism (disorder)
Hypopituitarism (disorder)
Isolated gonadotrophin deficiency
Deficiency in anterior pituitary function, variable immunodeficiency syndrome
Hypopituitarism due to pituitary tumor
Hypogonadism with anosmia (disorder)
Sexual ateleiotic dwarfism
Idiopathic hypogonadotropic hypogonadism
Kallmann syndrome
Pituitary deficiency due to empty sella turcica syndrome
Hypergonadotropic hypogonadism with cataract syndrome
Anosmia
Ateleiotic dwarfism
hypopituitary dwarfism
Hyposecretion Syndrome, Anterior Pituitary
Hypopituitarism following procedure
Immunodeficiency with major anomalies
Central hypothyroidism
Isolated GH Deficiency
hypogonadotrophic hypogonadism
Nebecourt syndrome
Postpartum Hypopituitarism
Deficient secretion of one OR more pituitary hormones
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
Congenital stenosis of carotid artery
RHYNS syndrome
Congenital malformation of anterior pituitary
Kallmann's Syndrome
Multiple pituitary hormone deficiency genetic form
Gonadotropin releasing hormone deficiency
primary hypopituitarism
Isolated gonadotropin deficiency
Pituitary nanism
Absent smell
kallman's syndrome
Pituitary dwarfism (disorder)
HYPOGONADOTROPIC HYPOGONADISM 23 WITH OR WITHOUT ANOSMIA
Primary hypergonadotropic hypogonadism and partial alopecia syndrome
LH - luteinizing hormone deficiency
Congenital anomaly of anterior pituitary
Amenorrhoea due to congenital gonadotrophin releasing hormone deficiency
Lubinsky syndrome
pituitary dwarf
sheehans syndrome
Sheehan's Syndrome
Congenital small nose
Cataract and testicular failure syndrome
Isolated growth hormone deficiency - autosomal dominant
Psychosocial growth hormone insufficiency
HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA
Autoimmune hypopituitarism
Hypogonadotropic Hypogonadism and Anosmia
Familial enlargement of the sella turcica
No sense of smell
HH23
Isolated follicle stimulating hormone deficiency
Autosomal dominant isolated somatotropin deficiency
Prepuberal panhypopituitarism
Pituitary dwarfism type I
Anaemia of endocrine disorder
Pituitary cachexia
Pituitary short stature
Hypogonadism with anosmia
Sequelae of endocrine disorders
Hypopituitarism due to disorder characterised by granuloma
Frohlich dwarfism
Loss of sense of smell
Anterior pituitary hormone deficiency
Isolated prolactin deficiency
Sheehan's syndrome (disorder)
Post-infarction hypopituitarism
Congenital facial nerve palsy
Devriendt Vandenberghe Fryns syndrome
Primary pituitary - hypothalamic infertility
Prepuberal dwarfism
Ferrier-Stone syndrome
Late-onset isolated adrenocorticotropic hormone deficiency
Congenital disorder of facial nerve
ANTERIOR PITUITARY HYPOSECRET SYNDROME
Hypopituitarism due to metabolic disease
Pituitary deficiency
Moyamoya disease
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
Amenorrhea due to congenital GnRH (gonadotrophin releasing hormone) deficiency
Hypoplasia of eye
Idiopathic growth hormone deficiency
Dwarfism, Pituitary
Isolated deficiency of pituitary hormone (disorder)
Hypogonadotropic Hypogonadism with Anosmia
Primary empty sella syndrome
Rudimentary eye
Immunoglobulinemia with isolated somatotropin deficiency
Hypogonadotropic hypogonadism due to luteinising hormone deficiency
Hypogonadotropic hypogonadism-anosmia syndrome
Moyamoya disease, short stature, facial dysmorphism, hypergonadotropic hypogonadism
Hypogonadotropic hypogonadism due to luteinizing hormone deficiency
Obesity, early-onset, adrenal insufficiency, and red hair
pituitary hypofunction
hypophyseal dwarf
Hyposomatotropic dwarfism
Post-infective hypopituitarism
GHD - Growth hormone deficiency
Isolated lutropin deficiency (disorder)
Loss of the sense of smell
Hypogonadisms, Anosmic
Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome
Combined pituitary hormone deficiency genetic form
Avascular necrosis of pituitary gland
SIMMONDS DIS
Hereditary growth hormone deficiency
Gonadotrophin releasing factor deficiency
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome
Mikati Najjar Sahli syndrome
Pituitary dwarfism with large sella turcica
GROWTH HORMONE DEFIC DWARFISM
Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency
Isolated HGH Deficiency
Kallman syndrome with cardiopathy
Necrosis of pituitary
Non-acquired combined pituitary hormone deficiency, deafness, rigid cervical spine syndrome
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome
Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome
Muscle disorders associated with endocrine disease
Pituitary cachexia (disorder)
Acquired central hypothyroidism due to disorder of pituitary gland
Nanism, Pituitary
Bosma arhinia microphthalmia syndrome
familial hypogonadism with anosmia
Bosma Henkin Christiansen syndrome
Kallman syndrome with heart disease
Acquired central hypothyroidism due to pituitary disorder
Lorain-Levi dwarfism
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome
Primary failure of the testes
Congenital hypoplasia of nose
Internal carotid artery stenosis
Isolated lutropin deficiency
Secondary hypopituitarism
Hypopituitarism due to disorder characterized by granuloma
Female infertility of pituitary - hypothalamic origin
Olfactogenital dysplasia
Secondary pituitary - hypothalamic infertility
Idiopathic pituitary dwarfism
Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency
Post-infective panhypopituitarism
Complete Hypopituitarism
Gonadotrophin deficiency
Hypoprolactinaemia
Functional hypogonadotropic hypogonadism
Sense of smell absent
Deficiency of gonadotropin releasing factor
Growth hormone insufficiency
Familial panhypopituitarism with abnormal sella turcica
Amenorrhoea due to Kallman syndrome
Isolated Human Growth Hormone Deficiency
Hypogonadism, Hypogonadotropic
Abnormal sella turcica syndrome
Ateliotic dwarfism without insulinopenia
Late-onset isolated ACTH deficiency
Hypopituitarism due to disorder of blood vessel
Hyposomatotrophic Dwarfism
Insufficiency, Pituitary
Anemia of pituitary deficiency
Deficient secretion of all pituitary hormones
Lorain - Levi dwarfism
deficiencies pituitary
Isolated deficiency of growth hormone
Autosomal recessive isolated somatotropin deficiency
Adult growth hormone deficiency with onset in childhood
Hypopituitarism secondary to head trauma
Growth hormone deficiency
Short stature co-occurrent and due to endocrine disorder
Malouf syndrome
Hypopituitarism due to granulomatous disease
Primary testicular failure
Panhypopituitarism - anterior and posterior
de morsier syndrome
Hypopituitarism due to vascular disorder
Ischemic pituitary necrosis
Idiopathic hypopituitarism
Gonadotropin releasing factor deficiency
Transient somatotropin deficiency
Growth hormone neurosecretory dysfunction
IGHD - Idiopathic growth hormone deficiency
Prepubertal dwarfism
HYPOSECRET SYNDROME ANTERIOR PITUITARY
Olfacto genital dysplasia
Deficiency of gonadotrophin releasing factor
Prolactin deficiency
Hypopituitarism due to empty sella turcica syndrome
Growth hormone deficiency with hypogammaglobulinaemia
Familial congenital hypopituitarism
Immunodeficiency associated with multiple organ system abnormalities

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.

How does E23.0 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hypopituitarism 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 E23.0?

E23.0 maps to the ICD-11 code: 5A61.0 (Hypopituitarism).

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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.