homocysteine level (19.1 umol/L), high, indicates increased CV risk ICD-9 Code: 270.4 Disturbances of sulphur-bearing amino-acid metabolism ICD-10 Code: E72.11 Homocystinuria Plan: Increased activity level, healthy diet, risk factor control *UTD Overview of Homocysteine Rosenson, et al. Liter ature review through April 2014
270.5. ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 270.4 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services.
Aug 12, 2011 · How would you code Elevated homocysteine levels icd 9? Thanks, Nalini CPC . btadlock1 Guest. Messages 1,502 Location Lubbock, TX Best answers 0. Aug 12, 2011 #2 naliniaapc said: hi, how would you code elevated homocysteine levels icd 9? Thanks, nalini cpc Click to expand... 270.4 . N. NaliniAAPC Expert. Messages 347 Best answers 0.
Elevated Lp (a) ICD-10-CM Diagnosis Code Z83.430 [convert to ICD-9-CM] Family history of elevated lipoprotein (a) Family history of elevated Lp (a) ICD-10-CM Diagnosis Code Z83.430. Family history of elevated lipoprotein (a) 2019 - New Code 2020 2021 2022 Billable/Specific Code POA Exempt. Applicable To.
Code | Description |
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83090 | HOMOCYSTEINE |
Under CMS National Coverage Policy - revised title for 42 CFR §410.32 ‘Indicates that diagnostic tests may only be ordered by the treating physician (or other treating practitioner acting within the scope of his or her license and Medicare requirements). Added title ‘Diagnostic Services Defined’ to CMS internet-only manual, Publication 100-02 Chapter 6 Section 20.4.1. Added title ‘Diagnosis Code Requirements’ to CMS internet-only manual Publication 100-08 Chapter 3 Section 3.4.1.3. Under Sources of Information and Basis for Decision – revised title of the eleventh article listed.
Homocysteine levels will be covered by Medicare to confirm vitamin B12 or folate deficiency.
Serum homocysteine levels for the evaluation of treatment of hyperhomocysteinemia in patients with CV risk factors will be denied as not medically necessary.
Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of cystathionine beta-synthase and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, scoliosis, arachnodactyly, muscle weakness, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of mental retardation, and a tendency to develop fibrosis of arteries, frequently complicated by cerebrovascular accidents and myocardial infarction. (from Adams et al., Principles of Neurology, 6th ed, p979)
An autosomal recessive inherited metabolic disorder caused by mutations in the cbs, mthfr, mtr, and mtrr genes. It is characterized by abnormalities in the methionine metabolism and is associated with deficiency of cystathionine synthase. It results in the accumulation of homocysteine in the serum.
The 2022 edition of ICD-10-CM E72.11 became effective on October 1, 2021.