ICD-10 Search Results for genetic-carrier-z14


ICD-10-CM CodeDescriptionCategoryValid for Submission
Z14Genetic carrierNot Valid
Z14.8Genetic carrier of other disease
Genetic disorder carrier; Genetic predisposition; Symptomatic form of fragile X syndrome in female carrier; Carrier of muscular dystrophy; Hemophilia carrier; Carrier of hereditary factor VIII deficiency disease; Carrier of hereditary factor VIII deficiency disease; Manifesting female carrier of X-linked muscular dystrophy; Manifesting female carrier of X-linked muscular dystrophy; Carrier of heritable cancer; Symptomatic carrier of hereditary factor VIII deficiency disease; Asymptomatic carrier of hereditary factor VIII deficiency disease; Carrier of hereditary factor IX deficiency disease; Carrier of Tay Sachs disease gene mutation; Carrier of sickle cell gene mutation; Genetic disorder carrier; Carrier of spinal muscular atrophy; Carrier of Bloom syndrome; Carrier of nonsyndromic deafness; Carrier of Charcot-Marie-Tooth disease; Carrier of galactosemia; Carrier of chromosome translocation; Carrier of beta thalassemia; Carrier of hemoglobinopathy C disorder; Carrier of chromosome disorder; Carrier of alpha thalassemia; Carrier of hemoglobinopathy E disorder; Carrier of fragile X chromosome; Carrier of classical phenylketonuria; Carrier of von Willebrand disease; Carrier of Duchenne muscular dystrophy; Carrier of hemoglobinopathy disorder; Carrier of glycogen storage disease; Carrier of Cowden syndrome; Carrier of mitochondrial defect; Carrier of hemochromatosis; Carrier of myotonic dystrophy; Carrier of familial adenomatous polyposis; Carrier of Becker muscular dystrophy; Carrier of Gaucher disease; Carrier of hemochromatosis HFE gene mutation; Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier; Carrier of high risk cancer mutation gene; Carrier of Canavan disease; Carrier of familial dysautonomia;
Valid