Z14.8
BillableGenetic carrier of other disease
Genetic carrier of other disease
Also Known As / Clinical Terms
SNOMED CT
- Hereditary disease32895009
- Inherited disease32895009
- Carrier of genetic disease47461006
- Genetic disorder carrier47461006
- Genetic predisposition47708004
- Familial disease111941005
- Haemophilia carrier191301000
- Hemophilia carrier191301000
- Carrier of hereditary factor VIII deficiency disease234441009
- Haemophilia A carrier234441009
- Hemophilia A carrier234441009
- X-linked muscular dystrophy with limb girdle distribution240047005
- Meryon muscular dystrophy240048000
- X-linked muscular dystrophy with abnormal dystrophin240048000
- Xp21-linked muscular dystrophy240048000
- Manifesting female carrier of X-linked muscular dystrophy240050008
- Finding of gastrointestinal hormone level365778009
- Gastrointestinal hormone level365778009
- Gastrointestinal hormone level - finding365778009
- Carrier of hereditary factor IX deficiency disease439242001
- Haemophilia B carrier439242001
- Hemophilia B carrier439242001
- Carrier of Tay Sachs disease gene mutation441646007
- Carrier of sickle cell gene mutation442018007
- Carrier of haemochromatosis HFE gene mutation736703007
- Carrier of hemochromatosis HFE gene mutation736703007
- Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier765197008
- Maternally inherited mitochondrial deoxyribonucleic acid disease1162975000
- Maternally inherited mitochondrial disease1162975000
- Maternally inherited mtDNA (mitochondrial deoxyribonucleic acid) disorder1162975000
- Hereditary alpha-tryptasaemia trait detected1296783008
- Hereditary alpha-tryptasemia trait detected1296783008
- Asymptomatic carrier of hereditary factor VIII deficiency disease328271000119104
- Carrier of Becker muscular dystrophy680035451000119103
- Carrier of Bloom syndrome559151051000119108
- Carrier of Canavan disease98311000119105
- Carrier of Charcot-Marie-Tooth disease66471000119106
- Carrier of Cowden syndrome66781000119102
- Carrier of Duchenne muscular dystrophy66731000119103
- Carrier of Fanconi anaemia group C494884791000119105
- Carrier of Fanconi anaemia of complementation group C494884791000119105
- Carrier of Fanconi anemia group C494884791000119105
- Carrier of Fanconi anemia of complementation group C494884791000119105
- Carrier of Gaucher disease697788021000119105
- Carrier of Joubert syndrome type 2754097021000119101
- Carrier of Joubert syndrome with oculorenal defect754097021000119101
- Carrier of cerebello-oculo-renal syndrome754097021000119101
- Carrier of NEB-related nemaline myopathy809087311000119106
- Carrier of Nebulin-related nemaline myopathy809087311000119106
- Carrier of Niemann-Pick disease type A964190521000119101
- Carrier of Usher syndrome type 1F218521311000119109
- Carrier of Usher syndrome type 2864990181000119100
- Usher syndrome type 2 carrier864990181000119100
- Carrier of Usher syndrome type 3906902831000119100
- Carrier of Von Hippel-Lindau syndrome66681000119107
- Carrier of alpha thalassaemia66621000119108
- Carrier of alpha thalassemia66621000119108
- Carrier of beta thalassaemia66551000119101
- Carrier of beta thalassemia66551000119101
- Carrier of chromosome disorder66611000119101
- Carrier of chromosome translocation66511000119102
- Carrier of classical phenylketonuria66701000119105
- Carrier of congenital cystic kidney disease66541000119103
- Carrier of polycystic kidney disease66541000119103
- Carrier of dihydrolipoamide dehydrogenase deficiency477380501000119109
- Carrier of maple syrup urine disease, type III477380501000119109
- Carrier of familial adenomatous polyposis67051000119108
- Carrier of familial combined hyperlipidaemia66461000119100
- Carrier of familial combined hyperlipidemia66461000119100
- Carrier of familial dysautonomia98421000119108
- Carrier of familial hypercholesterolaemia66481000119109
- Carrier of familial hypercholesterolemia66481000119109
- Carrier of fragile X chromosome66661000119103
- Carrier of galactosemia66501000119100
- Carrier of glycogen storage disease66771000119100
- Carrier of haemochromatosis66971000119103
- Carrier of hemochromatosis66971000119103
- Carrier of haemoglobinopathy C disorder66601000119104
- Carrier of hemoglobinopathy C disorder66601000119104
- Carrier of haemoglobinopathy E disorder66631000119106
- Carrier of hemoglobinopathy E disorder66631000119106
- Carrier of haemoglobinopathy disorder66751000119109
- Carrier of hemoglobinopathy disorder66751000119109
- Carrier of heritable cancer286481000119102
- Carrier of high risk cancer mutation gene90671000119109
- Carrier of maple syrup urine disease type IB584836011000119107
- Carrier of metabolic disorder66871000119108
- Carrier of mitochondrial defect66801000119103
- Carrier of mucolipidosis type IV195953191000119108
- Carrier of muscular dystrophy137511000119103
- Carrier of myotonic dystrophy67031000119102
- Carrier of neurogenetic disorder286471000119100
- Carrier of nonsyndromic deafness66411000119103
- Carrier of spinal muscular atrophy481462461000119102
- Carrier of spinocerebellar ataxia66921000119104
- Carrier of von Willebrand disease66721000119101
- Symptomatic carrier of hereditary factor VIII deficiency disease328261000119105
Frequently Asked Questions
What is ICD-10 code Z14.8?
ICD-10-CM code Z14.8 represents "Genetic carrier of other disease". It 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.
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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.