Diagnosis Code: Z15.89

Short Description: Genetic susceptibility to other disease

Long Description: Genetic susceptibility to other disease

The code Z15.89 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 susceptibility to disease (Z15)
      • Z15.89 Genetic susceptibility to other disease

This code is valid for unacceptable principal diagnosis

Code Version: 2022 ICD-10-CM

Synonyms

• Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
• Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
• Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation
• Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
• Dense body defect
• Familial platelet syndrome with predisposition to acute myelogenous leukemia
• Genetic susceptibility to genetic disorder
• Genetic susceptibility to genetic disorder
• Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation
• Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation
• Malignant hyperthermia genetic susceptibility
• Malignant hyperthermia genetic susceptibility
• Mendelian susceptibility to mycobacterial disease
• Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency
• Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
• Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency
• Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency
• Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency
• Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency
• Mendelian susceptibility to mycobacterial disease due to partial STAT1 deficiency
• Predisposition to invasive fungal disease due to CARD9 deficiency
• Susceptibility to infection due to TYK2 deficiency
• Uncertain genetic susceptibility to malignant hyperthermia due to CACNA1S gene mutation
• Uncertain malignant hyperthermia predisposition due to RyR1 gene mutation
• X-linked mendelian susceptibility to mycobacterial disease

Crosswalk Information

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

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