Hypopituitarism. E23.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM E23.0 became effective on October 1, 2018. This is the American ICD-10-CM version of E23.0 - other international versions of ICD-10 E23.0 may differ.
Diagnosis Index entries containing back-references to E89.3: Absence (of) (organ or part) (complete or partial) pituitary gland (congenital) Q89.2 ICD-10-CM Diagnosis Code Q89.2 Complication(s) (from) (of) endocrine E34.9 ICD-10-CM Diagnosis Code E34.9 Disorder (of) - see also Disease pituitary gland E23.7 ICD-10-CM Diagnosis Code E23.7
E23.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2021 edition of ICD-10-CM E23.0 became effective on October 1, 2020. This is the American ICD-10-CM version of E23.0 - other international versions of ICD-10 E23.0 may differ.
Diagnosis Index entries containing back-references to E23.0: Ahumada-del Castillo syndrome E23.0 Brissaud's infantilism or dwarfism E23.0 Cachexia R64 ICD-10-CM Diagnosis Code R64 Decrease (d) function pituitary (gland) (anterior) (lobe) E23.0 posterior E23.0 (lobe) ovary in hypopituitarism E23.0
ICD-10 code E23. 0 for Hypopituitarism is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .
Hypopituitarism is a rare disorder in which your pituitary gland fails to produce one or more hormones, or doesn't produce enough hormones. The pituitary gland is a kidney-bean-sized gland situated at the base of your brain.
Hypofunction and other disorders of the pituitary gland.
9: Endocrine disorder, unspecified.
Central hypothyroidism is much less common and is usually due to a tumor in the pituitary gland that disrupts its function and causes hypopituitarism. Hypopituitary patients may be deficient in one or more hormones, including thyroid hormone, growth hormone, cortisol, estrogen (women) or testosterone (men).
The pituitary makes hormones that are needed for normal body functions. When you do not have two or more of the pituitary hormones, it is known as hypopituitarism (hahy-poh-pi-too-i-tuh-riz-uh m). The lack of all pituitary hormones is known as panhypopituitarism.
TreatmentCorticosteroids. These drugs, such as hydrocortisone (Cortef) or prednisone (Rayos), replace the adrenal hormones that aren't being produced because of an adrenocorticotropic hormone (ACTH) deficiency. ... Levothyroxine (Levoxyl, Synthroid, others). ... Sex hormones. ... Growth hormone. ... Fertility hormones.
Excessive blood loss during or after delivery of a baby may affect the function of the pituitary gland, leading to a form of maternal hypopituitarism known as Sheehan syndrome (SS). Such extensive bleeding may reduce the blood flow to the pituitary gland causing the pituitary cells to be damaged or die (necrosis).
An E23 error code indicates there is an issue with the drain pump. This happens when the drain pump is blocked, clogged, or faulty.
9: Endocrine disorder, unspecified.
ICD-10 code R79. 89 for Other specified abnormal findings of blood chemistry is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .
R53. 81: “R” codes are the family of codes related to "Symptoms, signs and other abnormal findings" - a bit of a catch-all category for "conditions not otherwise specified". R53. 81 is defined as chronic debility not specific to another diagnosis.
It is also known as type i pituitary dwarfism. Human hypophysial dwarf is caused by a deficiency of human growth hormone during development. A genetically heterogeneous disorder caused by hypothalamic gnrh deficiency and olfactory nerve defects.
A form of dwarfism caused by complete or partial growth hormone deficiency, resulting from either the lack of growth hormone-releasing factor from the hypothalamus or from the mutations in the growth hormone gene (gh1) in the pituitary gland. It is also known as type i pituitary dwarfism.
The ICD code E230 is used to code Hypogonadism. Hypogonadism is a medical term which describes a diminished functional activity of the gonads – the testes and ovaries in males and females, respectively – that may result in diminished sex hormone biosynthesis. In layman's terms, it is sometimes called "interrupted stage 1 puberty".
Other hormones produced by the gonads which may be decreased by hypogonadism include progesterone, DHEA, anti-Müllerian hormone, activin, and inhibin. Spermatogenesis and ovulation in males and females, respectively, may be impaired by hypogonadism, which, depending on the degree of severity, may result in partial or complete infertility.
Low androgen (e.g., testosterone) levels are referred to as hypoandrogenism and low estrogen (e.g., estradiol) as hypoestrogenism, and may occur as symptoms of hypogonadism in both sexes, but are generally only diagnosed in males and females respectively.
Pickardt syndrome (also Pickardt's syndrome or Pickardt–Fahlbusch syndrome) denotes a rare form of tertiary hypothyroidism that is caused by interruption of the portal veins connecting hypothalamus and pituitary.
Use Additional Code note means a second code must be used in conjunction with this code. Codes with this note are Etiology codes and must be followed by a Manifestation code or codes.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E23.1. Click on any term below to browse the alphabetical index.
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code E23.1 and a single ICD9 code, 253.7 is an approximate match for comparison and conversion purposes.