Deficiency, deficient. methylenetetrahydrofolate reductase E72.12 (MTHFR) Disorder (of) - see also Disease. metabolism NOS E88.9. ICD-10-CM Diagnosis Code E88.9. Metabolic disorder, unspecified. 2016 2017 2018 2019 2020 2021 Billable/Specific Code. amino-acid E72.9. ICD-10-CM Diagnosis Code E72.9.
Methylenetetrahydrofolate reductase mutation. ICD-10-CM E72.12 is grouped within Diagnostic Related Group (s) (MS-DRG v38.0): 642 Inborn and other disorders of metabolism. Convert E72.12 to ICD-9-CM.
Diagnosis Index entries containing back-references to E72.12: Deficiency, deficient methylenetetrahydrofolate reductase E72.12 (MTHFR) Disorder (of) - see also Disease metabolism NOS E88.9 ICD-10-CM Diagnosis Code E88.9. Metabolic disorder, unspecified 2016 2017 2018 2019 Billable/Specific Code
Diagnosis Index entries containing back-references to E72.11: Cystathionine synthase deficiency E72.11 Disorder (of) - see also Disease amino-acid homocystinuria E72.11. metabolism NOS E88.9 ICD-10-CM Diagnosis Code E88.9 Homocystinemia, homocystinuria E72.11 Hyperhomocysteinemia E72.11
Names and CodesCondition:1Methylene tetrahydrofolate reductase deficiencySNOMED CT Code:341797007—5,10-Methylenetetrahydrofolate reductase deficiency UMLS CUI:4C0268615ICD-9-CM Code:5270.4—Disturbances of sulphur-bearing amino-acid metabolismICD-10-CM Code:6E72.12—Methylenetetrahydrofolate reductase deficiency2 more rows
Methylenetetrahydrofolate Reductase (MTHFR) Deficiency is the most common genetic cause of elevated levels of homocysteine in the plasma (hyperhomocysteinemia). The MTHFR enzyme plays an important role in processing amino acids, specifically, the conversion of homocysteine to methionine.
ICD-10-CM Code for Encounter for screening for genetic and chromosomal anomalies Z13. 7.
ICD-10 code D52. 9 for Folate deficiency anemia, unspecified is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .
The MTHFR mutation will also cause issues with detoxing properly, as well as issues with hormone balance and immune system function. It has been associated with autoimmune conditions such as fibromyalgia, Hashimoto's, and lupus.
Homocystinuria due to methylene tetrahydrofolate reductase (MTHFR) deficiency is a metabolic disorder characterised by neurological manifestations.
Chromosomal abnormality, unspecified Q99. 9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM Q99. 9 became effective on October 1, 2021.
CPT® 81420, Under Genomic Sequencing Procedures and Other Molecular Multianalyte Assays. The Current Procedural Terminology (CPT®) code 81420 as maintained by American Medical Association, is a medical procedural code under the range - Genomic Sequencing Procedures and Other Molecular Multianalyte Assays.
Sequencing-based non-invasive prenatal testing (NIPT) (CPT® codes 81420, 81507) to screen for fetal trisomy 13, 18 and 21 is considered medically necessary in a viable single or twin gestation pregnancy ≥ 10 weeks gestation.
Vitamin B-12 (82607) and folate (82746) can be tested up to four times per year for malabsorption syndromes (K90. 9) or deficiency disorders (D81. 818, D81. 819, E53.
Vitamin B12 deficiency anemia, unspecified D51. 9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM D51. 9 became effective on October 1, 2021.
2022 ICD-10-CM Diagnosis Code D52. 9: Folate deficiency anemia, unspecified.