Diagnosis Code R62.52
Information for Medical Professionals
Diagnostic Related Groups
The diagnosis code R62.52 is grouped in the following Diagnostic Related Group(s) (MS-DRG V35.0)
- 640 - MISCELLANEOUS DISORDERS OF NUTRITION, METABOLISM, FLUIDS AND ELECTROLYTES WITH MCC
- 641 - MISCELLANEOUS DISORDERS OF NUTRITION, METABOLISM, FLUIDS AND ELECTROLYTES WITHOUT MCC
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.
- 783.43 - Short stature
- Below expected growth rate
- Ear, patella, short stature syndrome
- Familial short stature
- General growth finding
- Genetic defect of hair shaft
- Growth retardation
- Has not grown in height
- Height below average
- Idiopathic short stature
- O/E - lack of growth
- O/E - short stature
- O/E -physiological development
- Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome
- Rachitic dwarf
- Retardation of physical development
- Short stature associated with bone marrow transplant
- Short stature disorder
- Short stature due to radiation therapy
- Short stature for age
- Short stature of childhood
- Short stature with valvular heart disease and characteristic facies syndrome
- Wellesley Carman French syndrome
Index of Diseases and Injuries
References found for the code R62.52 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.
- Lack of growth
- Physical retardation
- Short stature NOS
- 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.
- short stature due to endocrine disorder (E34.3)
Information for Patients
Does your child seem much shorter - or much taller - than other kids his or her age? It could be normal. Some children may be small for their age but still be developing normally. Some children are short or tall because their parents are.
But some children have growth disorders. Growth disorders are problems that prevent children from developing normal height, weight, sexual maturity or other features.
Very slow or very fast growth can sometimes signal a gland problem or disease.
The pituitary gland makes growth hormone, which stimulates the growth of bone and other tissues. Children who have too little of it may be very short. Treatment with growth hormone can stimulate growth.
People can also have too much growth hormone. Usually the cause is a pituitary gland tumor, which is not cancer. Too much growth hormone can cause gigantism in children, where their bones and their body grow too much. In adults, it can cause acromegaly, which makes the hands, feet and face larger than normal. Possible treatments include surgery to remove the tumor, medicines, and radiation therapy.
- Acromegaly (Medical Encyclopedia)
- Beckwith-Wiedemann syndrome (Medical Encyclopedia)
- Delayed growth (Medical Encyclopedia)
- Failure to thrive (Medical Encyclopedia)
- Gigantism (Medical Encyclopedia)
- Growth chart (Medical Encyclopedia)
- Growth hormone deficiency (Medical Encyclopedia)
- Growth hormone test (Medical Encyclopedia)
- Short stature (Medical Encyclopedia)