Diagnosis Code: Z14.8

Short Description: Genetic carrier of other disease

Long Description: Genetic carrier of other disease

The code Z14.8 is VALID for claim submission

Code Classification:

• Factors influencing health status and contact with health services (Z00–Z99)
  • Genetic carrier and genetic susceptibility to disease (Z14-Z15)
    • Genetic carrier (Z14)
      • Z14.8 Genetic carrier of other disease

This code is valid for unacceptable principal diagnosis

Code Version: 2022 ICD-10-CM

Synonyms

• Asymptomatic carrier of hereditary factor VIII deficiency disease
• Carrier of alpha thalassemia
• Carrier of Becker muscular dystrophy
• Carrier of beta thalassemia
• Carrier of Bloom syndrome
• Carrier of Canavan disease
• Carrier of Charcot-Marie-Tooth disease
• Carrier of chromosome disorder
• Carrier of chromosome translocation
• Carrier of classical phenylketonuria
• Carrier of Cowden syndrome
• Carrier of Duchenne muscular dystrophy
• Carrier of familial adenomatous polyposis
• Carrier of familial dysautonomia
• Carrier of fragile X chromosome
• Carrier of galactosemia
• Carrier of Gaucher disease
• Carrier of glycogen storage disease
• Carrier of hemochromatosis
• Carrier of hemochromatosis HFE gene mutation
• Carrier of hemoglobinopathy C disorder
• Carrier of hemoglobinopathy disorder
• Carrier of hemoglobinopathy E disorder
• Carrier of hereditary factor IX deficiency disease
• Carrier of hereditary factor VIII deficiency disease
• Carrier of hereditary factor VIII deficiency disease
• Carrier of heritable cancer
• Carrier of high risk cancer mutation gene
• Carrier of mitochondrial defect
• Carrier of muscular dystrophy
• Carrier of myotonic dystrophy
• Carrier of nonsyndromic deafness
• Carrier of sickle cell gene mutation
• Carrier of spinal muscular atrophy
• Carrier of Tay Sachs disease gene mutation
• Carrier of von Willebrand disease
• Familial disease
• Fragile X chromosome
• Fragile X syndrome
• Gastrointestinal hormone level - finding
• Genetic disorder carrier
• Genetic predisposition
• Hemophilia carrier
• Hereditary disease
• Manifesting female carrier of X-linked muscular dystrophy
• Manifesting female carrier of X-linked muscular dystrophy
• Maternally inherited mitochondrial deoxyribonucleic acid disease
• Symptomatic carrier of hereditary factor VIII deficiency disease
• Symptomatic form of fragile X syndrome in female carrier
• Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier
• X-linked muscular dystrophy with abnormal dystrophin
• X-linked muscular dystrophy with abnormal dystrophin
• X-linked muscular dystrophy with limb girdle distribution
• X-linked muscular dystrophy with limb girdle distribution

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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