V83.89 GENETIC CARRIER STAT NEC

Home > ICD-9 List > Supplementary classification of factors influencing health status and contact with health services > Genetics (V83-V84) > V83 Genetic carrier status > V83.89

Code Information

Diagnosis Code: V83.89

Short Description: Genetic carrier stat NEC

Long Description: Other genetic carrier status

Code Classification:

Supplementary classification of factors influencing health status and contact with health services (E)
- Genetics (V83-V84)
  - V83 Genetic carrier status
    - V83.89 Genetic carrier stat NEC

Code Version: 2015 ICD-9-CM

Synonyms

Carrier of hereditary factor IX deficiency disease
Carrier of sickle cell gene mutation
Carrier of Tay Sachs disease gene mutation
Manifesting female carrier of X-linked muscular dystrophy

References to Index of Diseases and Injuries

The code V83.89 has the following ICD-9-CM references to the Index of Diseases and Injuries

Carrier (suspected) of
- defective gene V83.89
- genetic defect V83.89

Defect, defective 759.9
- gene, carrier (suspected) of V83.89

Crosswalk Information

The code V83.89 converts into the following ICD-10 code(s):

ICD-9 Code		ICD-10 Code	ICD-10 Description
V83.89		Z14.8	Genetic carrier of other disease

This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code	ICD-9 Description
V83.01	Asymptomatic hemophilia A carrier
V83.02	Symptomatic hemophilia A carrier
V83.81	Cystic fibrosis gene carrier

This page was last updated on: 10/1/2014

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