Diagnosis Code E22.0
Information for Medical Professionals
The diagnosis code E22.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG v33.0)
- ENDOCRINE DISORDERS WITH MCC 643
- ENDOCRINE DISORDERS WITH CC 644
- ENDOCRINE DISORDERS WITHOUT CC/MCC 645
Convert to ICD-9 General 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.
- 253.0 - Acromegaly and gigantism (approximate) Approximate Flag
The approximate flag is on, indicating that the relationship between the code in the source system and the code in the target system is an approximate equivalent.
- Arthropathy associated with acromegaly
- Cutis verticis gyrata with acromegaloid phenotype
- Dermatosis of scalp
- Endocrine myopathy
- Eunuchoid gigantism
- Gigantism and acromegaly
- Gigantism due to somatostatin deficiency
- Hypermelanosis due to acromegaly
- Hypermelanosis due to endocrine disorder
- Hypersomatotropic gigantism
- Multiple malformation syndrome with early overgrowth
- Myopathy in acromegaly
- Neuropathy in acromegaly
- Overproduction of growth hormone
- Sotos' syndrome
- Testicular hyperfunction
Index of Diseases and Injuries
References found for the code E22.0 in the Index of Diseases and Injuries:
- Inclusion Terms: Inclusion terms
List of terms is included under some codes. These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of “other specified” codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- Overproduction of growth hormone
- Type 1 Excludes Notes: Type 1 Excludes Notes
A type 1 Excludes note is a pure excludes note. It means “NOT CODED HERE!” An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- constitutional gigantism (E34.4)
- constitutional tall stature (E34.4)
- increased secretion from endocrine pancreas of growth hormone-releasing hormone (E16.8)
Information for Patients
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
- ACTH blood test
- Empty sella syndrome
- Follicle-stimulating hormone (FSH) blood test
- Growth hormone stimulation test
- Luteinizing hormone (LH) blood test
- Pituitary infarction
Sotos syndrome Sotos syndrome is a disorder characterized by a distinctive facial appearance, overgrowth in childhood, and learning disabilities or delayed development of mental and movement abilities. Characteristic facial features include a long, narrow face; a high forehead; flushed (reddened) cheeks; and a small, pointed chin. In addition, the outside corners of the eyes may point downward (down-slanting palpebral fissures). This facial appearance is most notable in early childhood. Affected infants and children tend to grow quickly; they are significantly taller than their siblings and peers and have an unusually large head. However, adult height is usually in the normal range.People with Sotos syndrome often have intellectual disability, and most also have behavioral problems. Frequent behavioral issues include attention deficit hyperactivity disorder (ADHD), phobias, obsessions and compulsions, tantrums, and impulsive behaviors. Problems with speech and language are also common. Affected individuals often have a stutter, a monotone voice, and problems with sound production. Additionally, weak muscle tone (hypotonia) may delay other aspects of early development, particularly motor skills such as sitting and crawling.Other signs and symptoms of Sotos syndrome can include an abnormal side-to-side curvature of the spine (scoliosis), seizures, heart or kidney defects, hearing loss, and problems with vision. Some infants with this disorder experience yellowing of the skin and whites of the eyes (jaundice) and poor feeding.A small percentage of people with Sotos syndrome have developed cancer, most often in childhood, but no single form of cancer occurs most frequently with this condition. It remains uncertain whether Sotos syndrome increases the risk of specific types of cancer. If people with this disorder have an increased cancer risk, it is only slightly greater than that of the general population.