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Z14.8

Billable

Genetic carrier of other disease

Genetic carrier of other disease

Status

Billable / Specific

Block

Z14-Z15

Parent Code

Z14
Related Codes(2)
Z14.0

Hemophilia A carrier

Z14.1

Cystic fibrosis carrier

Billable
Also Known As / Clinical Terms(195)

SNOMED CT

UMLS

Clinical Terms

  • Carrier of polycystic kidney disease
  • Carrier of von Willebrand disease
  • Carrier of Usher syndrome type 1F
  • Carrier of mucolipidosis type IV
  • Carrier of familial dysautonomia
  • Carrier of hemoglobinopathy C disorder
  • Haemophilia carrier
  • Maternally inherited mitochondrial disease
  • Carrier of familial hypercholesterolaemia
  • Asymptomatic carrier of hereditary factor VIII deficiency disease
  • Carrier of Duchenne muscular dystrophy
  • Carrier of neurogenetic disorder
  • Carrier of beta thalassemia
  • Maternally inherited mtDNA (mitochondrial deoxyribonucleic acid) disorder
  • Carrier of Cowden syndrome
  • Carrier of Joubert syndrome type 2
  • Carrier of Usher syndrome type 2
  • Carrier of metabolic disorder
  • X-linked muscular dystrophy with abnormal dystrophin
  • Manifesting female carrier of X-linked muscular dystrophy
  • Hemophilia carrier
  • Carrier of galactosemia
  • Carrier of hereditary factor VIII deficiency disease
  • Carrier of high risk cancer mutation gene
  • Carrier of Tay Sachs disease gene mutation
  • Carrier of maple syrup urine disease, type III
  • Carrier of Bloom syndrome
  • Carrier of haemoglobinopathy E disorder
  • Carrier of alpha thalassaemia
  • Carrier of genetic disease
  • Carrier of Charcot-Marie-Tooth disease
  • Carrier of Usher syndrome type 3
  • Carrier of Von Hippel-Lindau syndrome
  • Carrier of mitochondrial defect
  • Carrier of familial adenomatous polyposis
  • Carrier of Canavan disease
  • Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier
  • Haemophilia A carrier
  • Carrier of NEB-related nemaline myopathy
  • Hemophilia B carrier
  • Hereditary alpha-tryptasaemia trait detected
  • Carrier of hemoglobinopathy E disorder
  • Gastrointestinal hormone level
  • Carrier of sickle cell gene mutation
  • Carrier of nonsyndromic deafness
  • Maternally inherited mitochondrial deoxyribonucleic acid disease
  • Carrier of hemoglobinopathy disorder
  • Genetic predisposition
  • Carrier of maple syrup urine disease type IB
  • Carrier of Becker muscular dystrophy
  • Carrier of glycogen storage disease
  • Carrier of beta thalassaemia
  • Carrier of Gaucher disease
  • Symptomatic carrier of hereditary factor VIII deficiency disease
  • Carrier of alpha thalassemia
  • Carrier of chromosome translocation
  • Carrier of spinal muscular atrophy
  • Carrier of haemochromatosis
  • Familial disease
  • Carrier of dihydrolipoamide dehydrogenase deficiency
  • Carrier of Fanconi anemia group C
  • Carrier of familial hypercholesterolemia
  • Carrier of chromosome disorder
  • Carrier of hemochromatosis HFE gene mutation
  • Xp21-linked muscular dystrophy
  • Inherited disease
  • Carrier of Joubert syndrome with oculorenal defect
  • Carrier of fragile X chromosome
  • Carrier of hemochromatosis
  • Carrier of Niemann-Pick disease type A
  • Hereditary disease
  • Carrier of Fanconi anaemia of complementation group C
  • Carrier of spinocerebellar ataxia
  • X-linked muscular dystrophy with limb girdle distribution
  • Carrier of Fanconi anemia of complementation group C
  • Carrier of heritable cancer
  • Carrier of haemochromatosis HFE gene mutation
  • Carrier of muscular dystrophy
  • Hereditary alpha-tryptasemia trait detected
  • Genetic disorder carrier
  • Carrier of myotonic dystrophy
  • Gastrointestinal hormone level - finding
  • Hemophilia A carrier
  • Carrier of Fanconi anaemia group C
  • Carrier of haemoglobinopathy disorder
  • Haemophilia B carrier
  • Carrier of haemoglobinopathy C disorder
  • Carrier of classical phenylketonuria
  • Finding of gastrointestinal hormone level
  • Carrier of cerebello-oculo-renal syndrome
  • Carrier of familial combined hyperlipidemia
  • Carrier of congenital cystic kidney disease
  • Usher syndrome type 2 carrier
  • Carrier of hereditary factor IX deficiency disease
  • Carrier of familial combined hyperlipidaemia
  • Carrier of Nebulin-related nemaline myopathy
  • Meryon muscular dystrophy
Frequently Asked Questions
What is the ICD-10 code for genetic carrier of other disease?

The ICD-10-CM code for genetic carrier of other disease is Z14.8. The full clinical description is "Genetic carrier of other disease". Z14.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Z14.8 mean?

ICD-10-CM code Z14.8 represents “Genetic carrier of other disease”. It is classified under Chapter 22: Factors Influencing Health Status and Contact With Health Services and is a billable/specific code that can be used on a claim.

Is Z14.8 a billable code?

Yes, Z14.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Z14.8 in?

Z14.8 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).

What SNOMED CT codes does Z14.8 map to?

Z14.8 maps to 65 SNOMED CT concepts: 328271000119104, 680035451000119103, 559151051000119108, 98311000119105, 66471000119106, and 60 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Z14.8?

Z14.8 is linked to 1 UMLS Concept Unique Identifier: C2910641. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Z14.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like genetic carrier of other disease affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Z14.8?

There is no direct ICD-11 mapping available for Z14.8 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.