ICD10 code of X-linked Hypophosphatemia (XLH) and ICD9 code
What is the ICD10 code for X-linked Hypophosphatemia (XLH)? And the ICD9 code for X-linked Hypophosphatemia (XLH)?
X-linked Hypophosphatemia (XLH) is a genetic disorder characterized by low levels of phosphate in the blood, leading to impaired bone growth and skeletal abnormalities. The ICD-10 code for XLH is M21.0, which falls under the category of "Other specified acquired deformities of limbs." Unfortunately, there is no specific ICD-9 code for XLH as it was replaced by ICD-10 in 2015.
X-linked Hypophosphatemia (XLH) ICD-10 Code: M21.0
X-linked Hypophosphatemia (XLH) ICD-9 Code: 275.3
X-linked Hypophosphatemia (XLH) is a rare genetic disorder that affects the bones and teeth. It is characterized by low levels of phosphate in the blood, leading to impaired bone mineralization and skeletal abnormalities. XLH is inherited in an X-linked dominant manner, meaning that the condition is more commonly seen in males, while females may exhibit milder symptoms.
The ICD-10 code for X-linked Hypophosphatemia is M21.0. This code falls under the category of "Other acquired deformities of limbs" in the ICD-10 coding system. It is important for healthcare providers to accurately assign this code when diagnosing and treating patients with XLH to ensure proper documentation and billing.
The ICD-9 code for X-linked Hypophosphatemia is 275.3. In the previous coding system, XLH was classified under "Disorders of phosphorus metabolism and phosphatases." Although ICD-9 codes are no longer used for billing purposes, they may still be referenced for historical or research purposes.
Diagnosing XLH typically involves a combination of clinical evaluation, laboratory tests, and genetic testing. Common symptoms of XLH include short stature, bowed legs, dental abnormalities, bone pain, and muscle weakness. The condition can vary in severity, with some individuals experiencing more pronounced skeletal deformities and complications.
Treatment for XLH aims to address the underlying phosphate imbalance and manage associated symptoms. This may involve the use of phosphate and vitamin D supplements to improve phosphate levels in the blood and promote proper bone mineralization. Other interventions, such as physical therapy and orthopedic interventions, may be necessary to manage skeletal abnormalities and improve mobility.
It is crucial for healthcare professionals to stay updated with the latest coding guidelines and use the appropriate ICD-10 code (M21.0) when documenting and treating patients with X-linked Hypophosphatemia. Accurate coding ensures proper communication, reimbursement, and statistical analysis related to this rare genetic disorder.
ICD-9-CM Diagnosis Code 275.3 (Disorders Of Phosphorus Metabolism)
Posted Aug 9, 2017 by Felipe Zúñiga 2650
