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ICD-10 Search Results for genetic-susceptibility-to-disease-z15
ICD-10-CM Code | Description | Category | Valid for Submission |
---|---|---|---|
Z15 | Genetic susceptibility to disease | Not Valid | |
Z15.8 | Genetic susceptibility to other disease | Not Valid | |
Z15.89 | Genetic susceptibility to other disease Uncertain genetic susceptibility to malignant hyperthermia due to CACNA1S gene mutation; Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation; Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation; Genetic susceptibility to genetic disorder; Genetic susceptibility to genetic disorder; Malignant hyperthermia genetic susceptibility; Malignant hyperthermia genetic susceptibility; Uncertain genetic susceptibility to malignant hyperthermia due to CACNA1S gene mutation; Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation; Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation; Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation; Mendelian susceptibility to mycobacterial disease; Susceptibility to infection due to TYK2 deficiency; Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency; Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency; Genetic susceptibility to genetic disorder; Genetic susceptibility to genetic disorder; X-linked mendelian susceptibility to mycobacterial disease; 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; 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 partial interferon gamma receptor 2 deficiency; Malignant hyperthermia genetic susceptibility; Malignant hyperthermia genetic susceptibility; Uncertain genetic susceptibility to malignant hyperthermia due to CACNA1S gene mutation; Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation; Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation; Uncertain malignant hyperthermia predisposition due to RyR1 gene mutation; Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation; Mendelian susceptibility to mycobacterial disease; Predisposition to invasive fungal disease due to CARD9 deficiency; Susceptibility to infection due to TYK2 deficiency; Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency; Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency; Genetic susceptibility to genetic disorder; Genetic susceptibility to genetic disorder; X-linked mendelian susceptibility to mycobacterial disease; 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; Familial platelet syndrome with predisposition to acute myelogenous leukemia; 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 partial interferon gamma receptor 2 deficiency; Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation; Mendelian susceptibility to mycobacterial disease; Predisposition to invasive fungal disease due to CARD9 deficiency; Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency; Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency; X-linked mendelian susceptibility to mycobacterial disease; 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; 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 partial interferon gamma receptor 2 deficiency; | Valid |