| Condition:1 | Methylene tetrahydrofolate reductase deficiency |
|---|---|
| SNOMED CT Code:3 | 41797007—5,10-Methylenetetrahydrofolate reductase deficiency UMLS CUI:4C0268615 |
| ICD-9-CM Code:5 | 270.4—Disturbances of sulphur-bearing amino-acid metabolism |
| ICD-10-CM Code:6 | E72.12—Methylenetetrahydrofolate reductase deficiency |
Some people have a genetic mutation in 1 or both of their MTHFR genes. People with a mutation in 1 MTHFR gene are are said to be heterozygous; if mutations are present in both genes, the person is said to be homozygous or compound heterozygous for the mutation(s).Jul 7, 2015
D68. 51 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 D68. 51 became effective on October 1, 2021.
ICD-10 code E72. 12 for Methylenetetrahydrofolate reductase deficiency is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .
ICD-10 code Z15. 89 for Genetic susceptibility to other disease is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
(HEH-teh-roh-ZY-gus JEE-noh-tipe) The presence of two different alleles at a particular gene locus. A heterozygous genotype may include one normal allele and one mutated allele or two different mutated alleles (compound heterozygote).
Gene expression is termed "monoallelic" when only one of the two copies of a gene is active, while the other is silent. Monoallelic expression is frequently initiated early in the development of an organism and stably maintained thereafter.
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
511238: Methylenetetrahydrofolate Reductase (MTHFR) Thermolabile Variant, DNA Analysis | Labcorp.
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.
Genetic susceptibility to other malignant neoplasm Z15. 09 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
ICD-10 code: P94. 2 Congenital hypotonia - gesund.bund.de.
ICD-10-CM codes for ADHD include: F90. 0, Attention-deficit hyperactivity disorder, predominantly inattentive type. F90.