ICD-10 Diagnosis Code E23.0

Hypopituitarism

Diagnosis Code E23.0

ICD-10: E23.0
Short Description: Hypopituitarism
Long Description: Hypopituitarism
This is the 2017 version of the ICD-10-CM diagnosis code E23.0

Valid for Submission
The code E23.0 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Endocrine, nutritional and metabolic diseases (E00–E90)
    • Disorders of other endocrine glands (E20-E35)
      • Hypofunction and other disorders of the pituitary gland (E23)

Information for Medical Professionals

Diagnostic Related Groups
The diagnosis code E23.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG V34.0)

  • 643 - ENDOCRINE DISORDERS WITH MCC
  • 644 - ENDOCRINE DISORDERS WITH CC
  • 645 - ENDOCRINE DISORDERS WITHOUT CC/MCC

Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

Synonyms
  • Adrenocorticotropic hormone deficiency
  • Adult growth hormone deficiency
  • Adult growth hormone deficiency with onset in childhood
  • Adult-onset growth hormone deficiency
  • Anemia of endocrine disorder
  • Anemia of pituitary deficiency
  • Anterior pituitary hormone deficiency
  • Asexual dwarfism
  • Ateleiotic dwarfism
  • Ateliotic dwarf
  • Atypical ichthyosis vulgaris with hypogonadism
  • Autosomal recessive isolated somatotropin deficiency
  • Cutaneous syndrome with ichthyosis
  • Endocrine myopathy
  • Female hypogonadotropic hypogonadism
  • Female infertility of pituitary - hypothalamic origin
  • Female Kallman's syndrome
  • Follicle stimulating hormone deficiency
  • Gonadotropin releasing factor deficiency
  • Growth hormone deficiency
  • Growth hormone deficiency after bone marrow transplant
  • Growth hormone neurosecretory dysfunction
  • Hypogonadism with anosmia
  • Hypogonadotropic hypogonadism
  • Hypogonadotropic hypogonadism
  • Hypogonadotropic hypogonadism
  • Hypogonadotropic hypogonadism
  • Hypogonadotropic hypogonadism
  • Hypogonadotropic hypogonadism
  • Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency
  • Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency
  • Hypogonadotropic hypogonadism due to luteinizing hormone deficiency
  • Hypophysitis
  • Hypopituitarism
  • Hypopituitarism due to pituitary tumor
  • 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
  • Isolated follitropin deficiency
  • Isolated gonadotropin deficiency
  • Isolated growth hormone deficiency - autosomal dominant
  • Isolated lutropin deficiency
  • Isolated prolactin deficiency
  • Isolated somatotropin deficiency
  • Limbic encephalitis
  • Luteinizing hormone deficiency
  • Lymphocytic hypopituitarism
  • Morbid obesity
  • Myopathy in hypopituitarism
  • Necrosis of pituitary
  • Nonfamilial asexual dwarfism
  • Nonfamilial hyperinsulinemic isolated somatotropin deficiency
  • Panhypopituitarism
  • Panhypopituitarism - anterior and posterior
  • Panhypopituitarism - X-linked
  • Partial growth hormone deficiency
  • Partial hypopituitarism
  • Pituitary cachexia
  • 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
  • Prepuberal panhypopituitarism
  • Primary pituitary - hypothalamic infertility
  • Proopiomelanocortin deficiency syndrome
  • Psychosocial growth hormone deficiency
  • Secondary hypopituitarism
  • Secondary pituitary - hypothalamic infertility
  • Sheehan's syndrome
  • Transient somatotropin deficiency

Index of Diseases and Injuries
References found for the code E23.0 in the Index of Diseases and Injuries:


Information for Patients


Pituitary Disorders

Your pituitary gland is a pea-sized gland at the base of your brain. The pituitary is the "master control gland" - it makes hormones that affect growth and the functions of other glands in the body.

With pituitary disorders, you often have too much or too little of one of your hormones. Injuries can cause pituitary disorders, but the most common cause is a pituitary tumor.

  • ACTH (cosyntropin) stimulation test (Medical Encyclopedia)
  • ACTH blood test (Medical Encyclopedia)
  • Empty sella syndrome (Medical Encyclopedia)
  • Follicle-stimulating hormone (FSH) blood test (Medical Encyclopedia)
  • Gigantism (Medical Encyclopedia)
  • Growth hormone stimulation test (Medical Encyclopedia)
  • Hypopituitarism (Medical Encyclopedia)
  • Luteinizing hormone (LH) blood test (Medical Encyclopedia)
  • Pituitary infarction (Medical Encyclopedia)


[Read More]

Isolated growth hormone deficiency Isolated growth hormone deficiency is a condition caused by a severe shortage or absence of growth hormone. Growth hormone is a protein that is necessary for the normal growth of the body's bones and tissues. Because they do not have enough of this hormone, people with isolated growth hormone deficiency commonly experience a failure to grow at the expected rate and have unusually short stature. This condition is usually apparent by early childhood.There are four types of isolated growth hormone deficiency differentiated by the severity of the condition, the gene involved, and the inheritance pattern.Isolated growth hormone deficiency type IA is caused by an absence of growth hormone and is the most severe of all the types. In people with type IA, growth failure is evident in infancy as affected babies are shorter than normal at birth.People with isolated growth hormone deficiency type IB produce very low levels of growth hormone. As a result, type IB is characterized by short stature, but this growth failure is typically not as severe as in type IA. Growth failure in people with type IB is usually apparent in early to mid-childhood.Individuals with isolated growth hormone deficiency type II have very low levels of growth hormone and short stature that varies in severity. Growth failure in these individuals is usually evident in early to mid-childhood. It is estimated that nearly half of the individuals with type II have underdevelopment of the pituitary gland (pituitary hypoplasia). The pituitary gland is located at the base of the brain and produces many hormones, including growth hormone.Isolated growth hormone deficiency type III is similar to type II in that affected individuals have very low levels of growth hormone and short stature that varies in severity. Growth failure in type III is usually evident in early to mid-childhood. People with type III may also have a weakened immune system and are prone to frequent infections. They produce very few B cells, which are specialized white blood cells that help protect the body against infection (agammaglobulinemia).
[Read More]

Combined pituitary hormone deficiency Combined pituitary hormone deficiency is a condition that causes a shortage (deficiency) of several hormones produced by the pituitary gland, which is located at the base of the brain. A lack of these hormones may affect the development of many parts of the body. The first signs of this condition include a failure to grow at the expected rate and short stature that usually becomes apparent in early childhood.People with combined pituitary hormone deficiency may have hypothyroidism, which is underactivity of the butterfly-shaped thyroid gland in the lower neck. Hypothyroidism can cause many symptoms, including weight gain and fatigue. Other features of combined pituitary hormone deficiency include delayed or absent puberty and lack the ability to have biological children (infertility). The condition can also be associated with a deficiency of the hormone cortisol. Cortisol deficiency can impair the body's immune system, causing individuals to be more susceptible to infection.Rarely, people with combined pituitary hormone deficiency have intellectual disability; a short, stiff neck; or underdeveloped optic nerves, which carry visual information from the eyes to the brain.
[Read More]
Previous Code
Previous Code E23
Next Code
E23.1 Next Code