Z14.8

Approximate Synonyms

• Alpha thalassemia carrier

• Beta thalassemia carrier

• Canavan disease inherited enzyme disorder) carrier

• Carrier of alpha thalassemia

• Carrier of beta thalassemia

• Carrier of canavan disease

• Carrier of charcot-marie-tooth disease

• Carrier of chromosome disorder

• Carrier of chromosome translocation

• Carrier of classical phenylketonuria

• Carrier of deafness

• Carrier of duchenne muscular dystrophy

• Carrier of familial adenomatous polyposis

• Carrier of familial dysautonomia

• Carrier of fragile x chromosome

• Carrier of galactosemia

• Carrier of glycogen storage disease

• Carrier of hemochromatosis

• Carrier of hemoglobinopathy c disorder

• Carrier of hemoglobinopathy disorder

• Carrier of hemoglobinopathy e disorder

• Carrier of heritable cancer

• Carrier of heritable disorder

• Carrier of high risk cancer mutation gene

• Carrier of metabolic disorder

• Carrier of mitochondrial defect

• Carrier of muscular dystrophy

• Carrier of myotonic dystrophy

• Carrier of neurogenetic disorder

• Carrier of tay sachs disease gene mutation

• Carrier of von willebrand disease

• Charcot-marie-tooth disease inherited nerve disease) carrier

• Chromosome disorder carrier

• Chromosome translocation abnormal structure of chromosomes) carrier

• Deafness carrier

• Duchenne muscular dystrophy carrier

• Familial adenomatous polyp benign tumor) carrier

• Familial dysautonomia malfunction of part of nervous system) carrier

• Fragile x inherited chromosome abnormality) carrier

• Galactosemia inherited enzyme disorder) carrier

• Genetic disorder carrier

• Glycogen storage disease carrier

• Hemochromatosis iron overload) carrier

• Hemoglobinopathy abnormal hemoglobin) carrier

• Hemoglobinopathy c abnormal hemoglobin) carrier

• Hemoglobinopathy e abnormal hemoglobin) carrier

• Hemophilia carrier

• Hereditary non-polyposis colon cancer gene mutation positive

• Heritable cancer carrier

• Heritable disorder carrier

• High risk cancer mutation carrier

• Lynch syndrome inherited condition causes high risk of colon cancer) gene mutation positive

• Metabolic disorder carrier

• Mitochondrial structure of cell) defect carrier

• Muscular dystrophy carrier

• Myotonic muscular dystrophy carrier

• Neurogenetic disorder carrier

• Phenylketonuria inherited enzyme disorder) carrier

• Supervision high risk pregnancy, factor v leiden

• Supervision of high risk pregnancy for factor v leiden heterozygote done

• Tay-sachs disease inherited brain degenerative disease) carrier

• Von willebrand disease blood clots too slowly) carrier

Present On Admission

• Z14.8

Details

• Z14.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• The 2023 edition of ICD-10-CM Z14.8 became effective on October 1, 2022.

• This is the American ICD-10-CM version of Z14.8 – other international versions of ICD-10 Z14.8 may differ.