ICD-10 Search Results for genetic-susceptibility-to-disease-z15


ICD-10-CM CodeDescriptionCategoryValid for Submission
Z15Genetic susceptibility to diseaseNot Valid
Z15.8Genetic susceptibility to other diseaseNot Valid
Z15.89Genetic 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