Z82.69 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Family history of diseases of the ms sys and connective tiss. The 2018/2019 edition of ICD-10-CM Z82.69 became effective on October 1, 2018.
Z83.49 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Family history of endo, nutritional and metabolic diseases. The 2019 edition of ICD-10-CM Z83.49 became effective on October 1, 2018.
Family history of other diseases of the musculoskeletal system and connective tissue. Z82.69 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM Z82.69 became effective on October 1, 2019.
Methylenetetrahydrofolate reductase deficiency. E72.12 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM E72.12 became effective on October 1, 2018. This is the American ICD-10-CM version of E72.12 - other international versions of ICD-10 E72.12 may differ.
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
Family history of other specified conditions Z84. 89 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 Z84. 89 became effective on October 1, 2021.
ICD-10 code Z13. 79 for Encounter for other screening for genetic and chromosomal anomalies is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
Z13. 88 - Encounter for screening for disorder due to exposure to contaminants. ICD-10-CM.
“Code Z86. 010, Personal history of colonic polyps, should be assigned when 'history of colon polyps' is documented by the provider. History of colon polyp specifically indexes to code Z86.
ICD-10 Code for Atherosclerotic heart disease of native coronary artery without angina pectoris- I25. 10- Codify by AAPC.
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.
81420: Fetal chromosomal aneuploidy (e.g., trisomy 21, monosomy X) genomic sequence analysis panel, circulating cell-free fetal DNA in maternal blood, must include analysis of chromosomes 13, 18, and 21.
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.
Code Z13. 89, encounter for screening for other disorder, is the ICD-10 code for depression screening.
0 - 17 years inclusiveZ00. 129 is applicable to pediatric patients aged 0 - 17 years inclusive.
9.
Family history of other diseases of the musculoskeletal system and connective tissue 1 Z82.69 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 Short description: Family history of diseases of the ms sys and connective tiss 3 The 2021 edition of ICD-10-CM Z82.69 became effective on October 1, 2020. 4 This is the American ICD-10-CM version of Z82.69 - other international versions of ICD-10 Z82.69 may differ.
Categories Z00-Z99 are provided for occasions when circumstances other than a disease, injury or external cause classifiable to categories A00 -Y89 are recorded as 'diagnoses' or 'problems'. This can arise in two main ways: