Diagnosis Code: E23.0

Short Description: Hypopituitarism

Long Description: Hypopituitarism

The code E23.0 is VALID for claim submission

Code Classification:

• Endocrine, nutritional and metabolic diseases (E00–E89)
  • Disorders of other endocrine glands (E20-E35)
    • Hypofunction and other disorders of the pituitary gland (E23)
      • E23.0 Hypopituitarism

Code Version: 2022 ICD-10-CM

Synonyms

• Acquired central hypothyroidism
• Acquired central hypothyroidism due to pituitary disorder
• Acquired central hypothyroidism due to Sheehan syndrome
• ACTH deficiency
• Adult growth hormone deficiency
• Adult growth hormone deficiency with onset in childhood
• Adult-onset growth hormone deficiency
• Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
• Amenorrhea due to congenital gonadotrophin releasing hormone deficiency
• Anemia of endocrine disorder
• Anemia of pituitary deficiency
• Anterior pituitary hormone deficiency
• Asexual dwarfism
• Ateleiotic dwarfism
• Ateliotic dwarfism without insulinopenia
• Autoimmune hypopituitarism
• Autosomal dominant isolated somatotropin deficiency
• Autosomal recessive isolated somatotropin deficiency
• Avascular necrosis of pituitary gland
• Axonal neuropathy
• Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
• Central hypothyroidism
• Combined pituitary hormone deficiency genetic form
• Congenital disorder of facial nerve
• Congenital facial nerve palsy
• Congenital hypogonadotropic hypogonadism
• Congenital hypoplasia of nose
• Congenital malformation of anterior pituitary
• Congenital stenosis of carotid artery
• Deficiency in anterior pituitary function, variable immunodeficiency syndrome
• Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome
• Endocrine myopathy
• Female hypogonadotropic hypogonadism
• Female infertility of pituitary - hypothalamic origin
• Follicle stimulating hormone deficiency
• Functional hypogonadotropic hypogonadism
• Gonadotropin releasing factor deficiency
• Growth hormone deficiency
• Growth hormone deficiency after bone marrow transplant
• Growth hormone neurosecretory dysfunction
• Hereditary growth hormone deficiency
• Hereditary growth hormone deficiency
• Hereditary sensory neuropathy
• Hypergonadotropic hypogonadism with cataract syndrome
• Hypogonadism with anosmia
• Hypogonadism with anosmia
• Hypogonadotropic hypogonadism
• Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency
• Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency
• Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency
• Hypogonadotropic hypogonadism due to luteinizing hormone deficiency
• Hypogonadotropic hypogonadism retinitis pigmentosa syndrome
• Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome
• Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
• Hypophysitis
• Hypopituitarism
• Hypopituitarism due to granulomatous disease
• Hypopituitarism due to metabolic disease
• Hypopituitarism due to pituitary tumor
• Hypopituitarism due to vascular disorder
• Hypopituitarism following procedure
• Hypoplasia of eye
• Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome
• Idiopathic growth hormone deficiency
• Idiopathic hypogonadotropic hypogonadism
• Idiopathic hypopituitarism
• Idiopathic panhypopituitarism
• Immunodeficiency associated with multiple organ system abnormalities
• Immunodeficiency with major anomalies
• Immunoglobulinemia with isolated somatotropin deficiency
• Internal carotid artery stenosis
• Isolated follicle stimulating hormone deficiency
• Isolated gonadotropin deficiency
• Isolated lutropin deficiency
• Isolated pituitary hormone deficiency
• Isolated prolactin deficiency
• Isolated somatotropin deficiency
• Kallman syndrome with heart disease
• Late-onset isolated adrenocorticotropic hormone deficiency
• LH - luteinizing hormone deficiency
• Loss of sense of smell
• Loss of sense of smell
• Lymphocytic hypopituitarism
• Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
• Martsolf syndrome
• Microcephalus, hypergonadotropic hypogonadism, short stature syndrome
• Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome
• Morbid obesity
• Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
• Moyamoya disease
• Myopathy in hypopituitarism
• Necrosis of pituitary
• Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome
• Nonfamilial asexual dwarfism
• Nonfamilial hyperinsulinemic isolated somatotropin deficiency
• Panhypopituitarism
• Panhypopituitarism
• Panhypopituitarism - anterior and posterior
• Partial growth hormone deficiency
• Partial hypopituitarism
• Partial loss of hair
• Peripheral axonal neuropathy
• Pituitary cachexia
• Pituitary deficiency due to empty sella turcica syndrome
• Pituitary dwarfism
• Pituitary dwarfism with large sella turcica
• Pituitary dwarfism with normal somatotropin level AND low somatomedin
• Pituitary dwarfism with small sella turcica
• Post-birth injury hypopituitarism
• Post-infarction hypopituitarism
• Post-infarction hypopituitarism
• Post-infarction panhypopituitarism
• Post-infective hypopituitarism
• Postpartum hypopituitarism
• Post-traumatic hypopituitarism
• Post-traumatic hypopituitarism
• Post-traumatic hypopituitarism
• Prepuberal panhypopituitarism
• Primary hypergonadotropic hypogonadism and partial alopecia syndrome
• Primary pituitary - hypothalamic infertility
• Primary testicular failure
• Proopiomelanocortin deficiency syndrome
• Psychosocial growth hormone deficiency
• RAB18 deficiency
• RHYNS syndrome
• Secondary hypopituitarism
• Secondary pituitary - hypothalamic infertility
• Sensory neuropathy
• Sequelae of endocrine disorders
• Sequelae of endocrine disorders
• Sheehan's syndrome
• Short stature co-occurrent and due to endocrine disorder
• Short stature co-occurrent and due to endocrine disorder
• Short stature co-occurrent and due to endocrine disorder
• Short stature co-occurrent and due to endocrine disorder
• Short stature co-occurrent and due to endocrine disorder
• Short stature co-occurrent and due to endocrine disorder
• Testicular hypofunction
• Transient somatotropin deficiency
• X-linked panhypopituitarism

Diagnostic Related Group(s)

The code E23.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Endocrine Disorders With Mcc (643)
• Endocrine Disorders With Cc (644)
• Endocrine Disorders Without Cc/mcc (645)

References to Index of Diseases and Injuries

The code E23.0 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • 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

Crosswalk Information

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This page was last updated on: 10/1/2023

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