2024 ICD-10-CM Diagnosis Code E83.31
Familial hypophosphatemia
- ICD-10-CM Code:
- E83.31
- ICD-10 Code for:
- Familial hypophosphatemia
- Is Billable?
- Yes - Valid for Submission
- Chronic Condition Indicator: [1]
- Chronic
- Code Navigator:
E83.31 is a billable diagnosis code used to specify a medical diagnosis of familial hypophosphatemia. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2023 through September 30, 2024.
Approximate Synonyms
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Autosomal dominant hypophosphatemic bone disease
- Autosomal dominant hypophosphatemic bone disease
- Autosomal dominant hypophosphatemic rickets
- Autosomal recessive hypophosphatemic bone disease
- Autosomal recessive hypophosphatemic bone disease
- Autosomal recessive hypophosphatemic rickets
- Autosomal recessive hypophosphatemic rickets
- Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis
- Dysplasia with defective mineralization
- Dysplasia with defective mineralization
- Dysplasia with defective mineralization
- Hereditary hypophosphatemic rickets with hypercalciuria
- Lesion of bone
- Lesion of bone
- Lesion of bone
- Phosphopenic type rickets
Clinical Classification
Clinical Category is Other specified and unspecified nutritional and metabolic disorders
- CCSR Category Code: END016
- Inpatient Default CCSR: Y - Yes, default inpatient assignment for principal diagnosis or first-listed diagnosis.
- Outpatient Default CCSR: Y - Yes, default outpatient assignment for principal diagnosis or first-listed diagnosis.
Tabular List of Diseases and Injuries
The following annotation back-references are applicable to this diagnosis code. The Tabular List of Diseases and Injuries is a list of ICD-10-CM codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more.
Inclusion Terms
Inclusion TermsThese 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.
- Vitamin D-resistant osteomalacia
- Vitamin D-resistant rickets
Type 1 Excludes
Type 1 ExcludesA 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.
- vitamin D-deficiency rickets E55.0
Index to Diseases and Injuries References
The following annotation back-references for this diagnosis code are found in the injuries and diseases index. The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10-CM code(s).
- - Disorder (of) - See Also: Disease;
- - metabolism NOS - E88.9
- - phosphorus - E83.30
- - hypophosphatemia - E83.39
- - familial - E83.31
- - hypophosphatemia - E83.39
- - phosphorus - E83.30
- - metabolism NOS - E88.9
- - Osteomalacia - M83.9
- - vitamin-D-resistant in adults - E83.31
- - carpus - E83.31
- - clavicle - E83.31
- - femur - E83.31
- - fibula - E83.31
- - finger - E83.31
- - humerus - E83.31
- - ilium - E83.31
- - ischium - E83.31
- - metacarpus - E83.31
- - metatarsus - E83.31
- - multiple sites - E83.31
- - neck - E83.31
- - pubic ramus - E83.31
- - radius - E83.31
- - rib - E83.31
- - scapula - E83.31
- - skull - E83.31
- - tarsus - E83.31
- - tibia - E83.31
- - toe - E83.31
- - ulna - E83.31
- - vertebra - E83.31
- - vitamin-D-resistant in adults - E83.31
Convert E83.31 to ICD-9-CM
- ICD-9-CM Code: 275.3 - Dis phosphorus metabol
Approximate Flag - The approximate mapping means there is not an exact match between the ICD-10 and ICD-9 codes and the mapped code is not a precise representation of the original code.
Patient Education
Metabolic Disorders
Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system break the food parts down into sugars and acids, your body's fuel. Your body can use this fuel right away, or it can store the energy in your body tissues, such as your liver, muscles, and body fat.
A metabolic disorder occurs when abnormal chemical reactions in your body disrupt this process. When this happens, you might have too much of some substances or too little of other ones that you need to stay healthy. There are different groups of disorders. Some affect the breakdown of amino acids, carbohydrates, or lipids. Another group, mitochondrial diseases, affects the parts of the cells that produce the energy.
You can develop a metabolic disorder when some organs, such as your liver or pancreas, become diseased or do not function normally. Diabetes is an example.
[Learn More in MedlinePlus]
Hereditary hypophosphatemic rickets
Hereditary hypophosphatemic rickets is a disorder related to low levels of phosphate in the blood (hypophosphatemia). Phosphate is a mineral that is essential for the normal formation of bones and teeth.
In most cases, the signs and symptoms of hereditary hypophosphatemic rickets begin in early childhood. The features of the disorder vary widely, even among affected members of the same family. Mildly affected individuals may have hypophosphatemia without other signs and symptoms. More severely affected children experience slow growth and are shorter than their peers. They develop bone abnormalities that can interfere with movement and cause bone pain. The most noticeable of these abnormalities are bowed legs or knock knees. These abnormalities become apparent with weight-bearing activities such as walking. If untreated, they tend to worsen with time.
Other signs and symptoms of hereditary hypophosphatemic rickets can include premature fusion of the skull bones (craniosynostosis) and dental abnormalities. The disorder may also cause abnormal bone growth where ligaments and tendons attach to joints (enthesopathy). In adults, hypophosphatemia is characterized by a softening of the bones known as osteomalacia.
Researchers have described several forms of hereditary hypophosphatemic rickets, which are distinguished by their pattern of inheritance and genetic cause. The most common form of the disorder is known as X-linked hypophosphatemic rickets (XLH). It has an X-linked dominant pattern of inheritance. X-linked recessive, autosomal dominant, and autosomal recessive forms of the disorder are much rarer.
Another rare type of the disorder is known as hereditary hypophosphatemic rickets with hypercalciuria (HHRH). In addition to hypophosphatemia, this condition is characterized by the excretion of high levels of calcium in the urine (hypercalciuria).
[Learn More in MedlinePlus]
Code History
- FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
- FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
- FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
- FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
- FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
- FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
- FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
- FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
- FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.