R89.8
BillableOth abnormal findings in specimens from oth org/tiss
Other abnormal findings in specimens from other organs, systems and tissues
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Abnormal chromosomal findings in specimens from other organs, systems and tissues
Includes
Conditions included under this code
- abnormal findings in nipple discharge
- abnormal findings in synovial fluid
- abnormal findings in wound secretions
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- abnormal findings on antenatal screening of mother (O28.-)
- diagnostic abnormal findings classified elsewhere - see Alphabetical Index
Excludes 2
Conditions not included here, but the patient may have both
- abnormal findings on antenatal screening of mother (O28.-)
- certain conditions originating in the perinatal period (P04-P96)
- signs and symptoms classified in the body system chapters
- signs and symptoms of breast (N63, N64.5)
- abnormal findings on examination of blood, without diagnosis (R70-R79)
- abnormal findings on examination of urine, without diagnosis (R80-R82)
- abnormal tumor markers (R97.-)
Also Known As / Clinical Terms
SNOMED CT
- Increased molecular dissociation1777007
- Abnormal presence of haemoglobin3720003
- Abnormal presence of hemoglobin3720003
- Increased lactic acid level7501002
- Lactic acid level above reference range7501002
- Abnormal presence of myoglobin9437001
- Laxity12554006
- Laxness12554006
- Gene amplification12645001
- Genetic linkage equilibrium13300001
- Abnormal presence of protein13930000
- Abnormal thickness14028006
- Abnormal macromolecular binding15212002
- Abnormal presence of galactose15268006
- Depolymerisation16315008
- Depolymerization16315008
- Genetic mosaic17523003
- Decrease in circumference18250007
- Abnormally hard consistency19730000
- Hardening19730000
- Decreased size19776001
- Diminution of size19776001
- Inequality in circumference24122006
- Increased urobilinogen level24390000
- Urobilinogen level above reference range24390000
- Abnormal nucleotide base sequence25194005
- Gene re-arrangement, B lymphocyte, heavy chain25900007
- Positive skin test reaction26576000
- Molecular degradation28166001
- Abnormal nucleic acid sequence29286002
- Abnormal molecular cross-linking30453001
- Abnormal presence of glucose31649001
- Macromolecular defective synthesis33002009
- Abnormally soft consistency36350006
- Molecular dissociation36597008
- Retraction37794007
- Increased translucency38638004
- Rarefaction38638004
- Denaturation40241000
- Genetic linkage disequilibrium40976007
- Abnormal amniotic fluid42170009
- Amniotic fluid abnormal42170009
- Gene re-arrangement43245005
- Nucleic acid conformation43996000
- Increase in circumference44832008
- Decreased macromolecular binding44880006
- Strand breaks49030004
- Abnormal presence of pentose51028009
- Increased diameter51381009
- Conformational change52828007
- Macromolecular alteration52828007
- Macromolecular binding53586009
- Genetic mutation55446002
- Increase of specific gravity55759009
- Specific gravity above reference range55759009
- Allelic exclusion60181007
- Genetic inversion60844005
- Gene re-arrangement, gamma chain, T cell antigen receptor61668005
- Decreased uric acid level63192007
- Uric acid level below reference range63192007
- Genetic variation64195000
- Gene re-arrangement, T lymphocyte65247007
- Macromolecular nicking65264005
- Abnormal size65476007
- Molecular instability66115002
- Unstable molecule66115002
- Protein conformation66251001
- Carbohydrate conformation68036007
- Glucose level above reference range68256003
- Increased glucose level68256003
- DNA damage68349007
- DNA injury68349007
- Deoxyribonucleic acid damage68349007
- Cortical blindness68574006
- Abnormal amino acid sequence69604007
- Gene re-arrangement, alpha chain, T cell antigen receptor72644000
- Molecular inactivation72959009
- Shrinkage73238002
- Superhelicity76602008
- Gene re-arrangement, beta chain, T cell antigen receptor78473004
- Abnormal macromolecular sequence79667004
- Macromolecular cleavage81479001
- Abnormal translucency83484004
- Abnormal consistency86991001
- Increased macromolecular binding87523007
- Gene re-arrangement, B lymphocyte87682005
- Decreased translucency87956004
- Decreased molecular dissociation88668007
- Gene re-arrangement, B lymphocyte, light chain89017001
- Abnormal carbohydrate sequence89744004
- Defective molecular assembly89936009
- Molecular conformation90578002
- Acellular smear103607002
- Smear too thick for optimal interpretation103611008
- Specimen too thick for optimal interpretation103611008
- Translucency finding107648000
- Abnormal bone marrow iron110371003
- Absent bone marrow iron110374006
- Extra chromosomal inheritance112212006
- Sample lipaemic118127007
- Sample lipemic118127007
- Specimen lipaemic118127007
- Specimen lipemic118127007
- Sample haemolysed118128002
- Sample hemolyzed118128002
- Specimen haemolysed118128002
- Specimen hemolyzed118128002
- Sample icteric118129005
- Specimen icteric118129005
- Finding by inspection (simple observation)118243007
- Satisfactory for evaluation but limited by partially obscuring thick areas123833004
- Increased ketone bodies123984002
- Ketone bodies above reference range123984002
- Increased orotic acid123986000
- Orotic acid above reference range123986000
- Decreased orotic acid123987009
- Orotic acid below reference range123987009
- Increased xanthine123990003
- Xanthine above reference range123990003
- Decreased xanthine123991004
- Xanthine below reference range123991004
- Homogentisic acid above reference range123993001
- Increased homogentisic acid123993001
- Carbohydrate above reference range123995008
- Increased carbohydrate123995008
- Carbohydrate below reference range123996009
- Decreased carbohydrate123996009
- Fructose above reference range123997000
- Increased fructose123997000
- Decreased fructose123998005
- Fructose below reference range123998005
- Increased lactose124000000
- Lactose above reference range124000000
- Decreased lactose124001001
- Lactose below reference range124001001
- Galactose above reference range124003003
- Increased galactose124003003
- Decreased galactose124004009
- Galactose below reference range124004009
- Increased mannoheptulose124006006
- Mannoheptulose above reference range124006006
- Decreased mannoheptulose124007002
- Mannoheptulose below reference range124007002
- Increased pentose124008007
- Pentose above reference range124008007
- Decreased pentose124009004
- Pentose below reference range124009004
- Glycogen above reference range124011008
- Increased glycogen124011008
- Decreased glycogen124012001
- Glycogen below reference range124012001
- Increased methaemalbumin124016003
- Increased methemalbumin124016003
- Methaemalbumin above reference range124016003
- Methemalbumin above reference range124016003
- Decreased methaemalbumin124017007
- Decreased methemalbumin124017007
- Methaemalbumin below reference range124017007
- Methemalbumin below reference range124017007
- Decreased globulin124020004
- Globulin below reference range124020004
- Decreased protein-bound iodine124030008
- Protein-bound iodine below reference range124030008
- Increased ceroid124038001
- Decreased ceroid124039009
- Abnormal structure of phospholipid124044002
- Abnormal structure of cerebroside124049007
- Amino acid above reference range124056001
- Increased amino acid124056001
- Amino acid below reference range124057005
- Decreased amino acid124057005
- Beta amino isobutyric acid above reference range124059008
- Increased beta amino isobutyric acid124059008
- Beta amino isobutyric acid below reference range124060003
- Decreased beta amino isobutyric acid124060003
- Cystine above reference range124061004
- Increased cystine124061004
- Cystine below reference range124062006
- Decreased cystine124062006
- Histidine above reference range124063001
- Increased histidine124063001
- Decreased histidine124064007
- Histidine below reference range124064007
- Increased tyrosine124065008
- Tyrosine above reference range124065008
- Decreased tyrosine124066009
- Tyrosine below reference range124066009
- Decreased porphyrin124068005
- Porphyrin below reference range124068005
- Decreased uroporphyrin124071002
- Uroporphyrin below reference range124071002
- Bilirubin level below reference range124078008
- Decreased bilirubin level124078008
- Biliverdin above reference range124080002
- Increased biliverdin124080002
- Decreased urobilinogen level124082005
- Urobilinogen level below reference range124082005
- Increased urobilin124085007
- Urobilin above reference range124085007
- Decreased urobilin124086008
- Urobilin below reference range124086008
- Adenylic acid above reference range124088009
- Increased adenosine monophosphate124088009
- Increased adenylic acid124088009
- Adenylic acid below reference range124089001
- Decreased adenosine monophosphate124089001
- Decreased adenylic acid124089001
- Alteration of genetic material124972006
- Somatic mutation124975008
- Temperature-sensitive mutation124976009
- Nucleotide base deletion124977000
- Cell division alteration124978005
- Mitotic alteration124979002
- Increased cell mitotic activity124980004
- Decreased cell mitotic activity124981000
- Mitotic arrest124982007
- Meiotic alteration124988006
- Finding of organ weight125123008
- Abnormal organ weight125125001
- Abnormally increased organ weight125126000
- Abnormally decreased organ weight125127009
- Satisfactory for evaluation but limited by partially obscuring air drying artefact125158005
- Satisfactory for evaluation but limited by partially obscuring air drying artifact125158005
- Choline above reference range127351006
- Increased choline127351006
- Choline below reference range127352004
- Decreased choline127352004
- Finding related to physiologic substance127357005
- Abnormal structure of physiologic substance127359008
- Abnormal quantity of physiologic substance127360003
- Quantity of physiologic substance outside reference range127360003
- Increased vanillylmandelic acid level131040000
- Vanillylmandelic acid level above reference range131040000
- Decreased vanillylmandelic acid level131041001
- Vanillylmandelic acid level below reference range131041001
- Decreased thyroid hormone level131090001
- Thyroid hormone level below reference range131090001
- Increased vitamin A131109009
- Vitamin A above reference range131109009
- Increased vitamin D131113002
- Vitamin D above reference range131113002
- Increased vitamin E131115009
- Vitamin E above reference range131115009
- Increased vitamin K131116005
- Vitamin K above reference range131116005
- Decreased vitamin B131125004
- Vitamin B below reference range131125004
- Increased vitamin B12131126003
- Vitamin B12 above reference range131126003
- Ascorbic acid above reference range131128002
- Increased ascorbic acid131128002
- Increased vitamin C131128002
- Ascorbic acid below reference range131129005
- Decreased ascorbic acid131129005
- Decreased vitamin C131129005
- Folic acid above reference range131132008
- Increased folic acid131132008
- Decreased folic acid131133003
- Folic acid below reference range131133003
- Decreased fibrinogen131177005
- Fibrinogen below reference range131177005
- Monocyte count abnormal165541006
- Monocyte count outside reference range165541006
- AFP - Alpha-fetoprotein raised166561008
- Alpha-fetoprotein above reference range166561008
- Alpha-fetoprotein raised166561008
- Protein electrophoresis abnormal166803003
- Protein electrophoresis outside reference range166803003
- Joint fluid yellow167881006
- Synovial fluid yellow167881006
- Joint fluid cloudy167882004
- Synovial fluid cloudy167882004
- Joint fluid turbid167884003
- Synovial fluid turbid167884003
- Synovial fluid viscosity high167888000
- Synovial fluid viscosity low167889008
- Synovial fluid fibrin clot167891000
- Synovial fluid: fibrin clot +167893002
- Synovial fluid: abnormal content167899003
- Synovial fluid: crystals167902000
- Synovial fluid: uric acid167903005
- Synovial fluid: pyrophosphate167904004
- Bone marrow normoblastic167920009
- Bone marrow megaloblastic167921008
- Bone marrow erythropoiesis hyperplasia167922001
- Calculus = carbaptite168072004
- Calculus = hydroxyapatite168073009
- Calculus = phosphate168075002
- Calculus = cholesterol168077005
- Calculus = bilirubin168078000
- Calculus = triple phosphate168079008
- Amniotic fluid AFP (alpha-fetoprotein) abnormal168109006
- Amniotic fluid alpha-fetoprotein abnormal168109006
- Amniotic fluid alpha-fetoprotein outside reference range168109006
- Cell chromosome examination abnormal168448002
- Amount of liquor249131000
- Finding of amniotic fluid volume249131000
- Finding of quantity of amniotic fluid249131000
- Finding of quantity of liquor249131000
- Observation of quantity of liquor249131000
- Quantity of liquor249131000
- Cold agglutinins detected250256002
- Cold agglutinins present250256002
- Stringing of synovial fluid250534004
- Snowstorm knee250535003
- GU test finding251409007
- GU test observation251409007
- Genitourinary test finding251409007
- Vesicular reaction252100001
- Mucopurulent263815005
- Blood in synovial fluid269909003
- Joint fluid bloody269909003
- Joint fluid haemorrhagic269909003
- Joint fluid hemorrhagic269909003
- Synovial fluid bloodstained269909003
- Phosphate calculus of kidney275893001
- Phosphate kidney stone275893001
- Sample grossly haemolysed281288006
- Sample grossly hemolyzed281288006
- Specimen grossly haemolysed281288006
- Specimen grossly hemolyzed281288006
- Sample slightly haemolysed281289003
- Sample slightly hemolyzed281289003
- Specimen slightly haemolysed281289003
- Specimen slightly hemolyzed281289003
- Sample slightly icteric281290007
- Specimen slightly icteric281290007
- Sample grossly icteric281291006
- Specimen grossly icteric281291006
- Sample grossly lipaemic281292004
- Sample grossly lipemic281292004
- Specimen grossly lipaemic281292004
- Specimen grossly lipemic281292004
- Sample slightly lipaemic281293009
- Sample slightly lipemic281293009
- Specimen slightly lipaemic281293009
- Specimen slightly lipemic281293009
- Aceto-white reaction positive300557001
- Addition-deletion mutation325753009
- Frame-shift mutation325753009
- Reading-frame-shift mutation325753009
- Suppressor mutation326724004
- Nonsense mutation327671006
- Abnormally increased laxity359733004
- Abnormally increased laxness359733004
- Increased laxity359733004
- Increased laxness359733004
- Finding of vitamin B12 level365604004
- Vitamin B12 level365604004
- Finding of monocyte count365631001
- Monocyte count365631001
- Monocyte count - finding365631001
- Finding of presence of crystals365687009
- Presence of crystals365687009
- Presence of crystals - finding365687009
- Finding of presence of ova cysts and parasites365694007
- Presence of ova cysts and parasites365694007
- Presence of ova cysts and parasites - finding365694007
- Finding of synovial fluid viscosity365710005
- Synovial fluid viscosity - finding365710005
- Finding of synovial fluid composition365711009
- Synovial fluid composition - finding365711009
- Finding of synovial fluid appearance365712002
- Bilirubin level365786009
- Bilirubin level - finding365786009
- Finding of bilirubin level365786009
- Calculus chemical composition365789002
- Calculus chemical composition - finding365789002
- Finding of calculus chemical composition365789002
- Amniotic fluid AFP365827005
- Amniotic fluid AFP - finding365827005
- Finding of amniotic fluid alpha-fetoprotein365827005
- Finding of specific gravity365828000
- Specific gravity365828000
- Specific gravity - finding365828000
- Finding of bone marrow erythropoiesis365835008
- Aceto-white reaction finding366318009
- Contact sensitivity response - finding366665009
- Finding of contact sensitivity response366665009
- Fragmented tissue specimen395528004
- Tissue specimen fragmented395528004
- Tissue specimen ruptured397332005
- Fetal tissue present in specimen397475000
- Foetal tissue present in specimen397475000
- Fetal anomaly present in specimen405999008
- Foetal anomaly present in specimen405999008
- Genetic finding detected412731001
- Positive genetic finding412731001
- Bone marrow iron finding413680005
- Granulocyte count below reference range416955003
- Granulopenia416955003
- Mitochondrial mutation430934002
- Cholesterol/high density lipoprotein ratio above reference range439953004
- Elevated cholesterol/high density lipoprotein ratio439953004
- Influenza A virus subtype H1 detected441043003
- Influenza A virus subtype H1 present441043003
- Karyotype evaluation abnormal442124003
- Measurement finding below reference range442686002
- Measurement finding above reference range442756004
- Cancer antigen 27-29 above reference range444764006
- High cancer antigen 27-29 level444764006
- Specimen involvement by multifocal invasion444902000
- Breast cancer genetic marker of susceptibility detected445333001
- Breast cancer genetic marker of susceptibility positive445333001
- Effect of antiestrogen agent445963000
- Effect of antioestrogen agent445963000
- Finding of oxygen saturation447755005
- Point mutation471281007
- Influenza A H1N1 virus 2009 pandemic strain present702482001
- Mitochondrial 1555 A to G mutation detected702782002
- Mitochondrial 1555 A to G mutation positive702782002
- Heterozygous protocadherin 19 gene mutation detected702783007
- Heterozygous protocadherin 19 gene mutation positive702783007
- Suture material present718569006
- Mutation of p53 gene719007008
- Mutation of p53 gene present719007008
- Positive for tumor protein p53719007008
- Positive for tumour protein p53719007008
- Tumor protein p53 detected719007008
- Tumour protein p53 detected719007008
- Needle shaped crystals present720353000
- CYP2C9 poor metaboliser738545001
- CYP2C9 poor metabolizer738545001
- Cytochrome P450 family 2 subfamily C member 9 poor metaboliser738545001
- Cytochrome P450 family 2 subfamily C member 9 poor metabolizer738545001
- CYP2C19 rapid metaboliser738789003
- CYP2C19 rapid metabolizer738789003
- Cytochrome P450 family 2 subfamily C member 19 rapid metaboliser738789003
- Cytochrome P450 family 2 subfamily C member 19 rapid metabolizer738789003
- CMMR-D (constitutional mismatch repair deficiency) syndrome764946008
- Constitutional mismatch repair deficiency syndrome764946008
- VKORC1 (vitamin K epoxide reductase complex 1) poor metaboliser787128002
- VKORC1 (vitamin K epoxide reductase complex 1) poor metabolizer787128002
- VKORC1 poor metaboliser787128002
- VKORC1 poor metabolizer787128002
- Vitamin K epoxide reductase complex 1 poor metaboliser787128002
- Vitamin K epoxide reductase complex 1 poor metabolizer787128002
- VKORC1 (vitamin K epoxide reductase complex 1) rapid metaboliser787133003
- VKORC1 (vitamin K epoxide reductase complex 1) rapid metabolizer787133003
- VKORC1 rapid metaboliser787133003
- VKORC1 rapid metabolizer787133003
- Vitamin K epoxide reductase complex 1 rapid metaboliser787133003
- Vitamin K epoxide reductase complex 1 rapid metabolizer787133003
- VKORC1 (vitamin K epoxide reductase complex 1) ultra-rapid metaboliser787134009
- VKORC1 (vitamin K epoxide reductase complex 1) ultra-rapid metabolizer787134009
- VKORC1 ultra-rapid metaboliser787134009
- VKORC1 ultra-rapid metabolizer787134009
- Vitamin K epoxide reductase complex 1 ultra-rapid metaboliser787134009
- Vitamin K epoxide reductase complex 1 ultra-rapid metabolizer787134009
- CYP2C9 (cytochrome P450 family 2 subfamily C member 9) ultra-rapid metaboliser787192006
- CYP2C9 (cytochrome P450 family 2 subfamily C member 9) ultra-rapid metabolizer787192006
- CYP2C9 ultra-rapid metaboliser787192006
- CYP2C9 ultra-rapid metabolizer787192006
- Cytochrome P450 family 2 subfamily C member 9 ultra-rapid metaboliser787192006
- Cytochrome P450 family 2 subfamily C member 9 ultra-rapid metabolizer787192006
- CYP2C9 (cytochrome P450 family 2 subfamily C member 9) rapid metaboliser787193001
- CYP2C9 (cytochrome P450 family 2 subfamily C member 9) rapid metabolizer787193001
- CYP2C9 rapid metaboliser787193001
- CYP2C9 rapid metabolizer787193001
- Cytochrome P450 family 2 subfamily C member 9 rapid metaboliser787193001
- Cytochrome P450 family 2 subfamily C member 9 rapid metabolizer787193001
- CYP1A2 (cytochrome P450 family 1 subfamily A member 2) poor metaboliser787363003
- CYP1A2 (cytochrome P450 family 1 subfamily A member 2) poor metabolizer787363003
- CYP1A2 poor metaboliser787363003
- CYP1A2 poor metabolizer787363003
- Cytochrome P450 family 1 subfamily A member 2 poor metaboliser787363003
- Cytochrome P450 family 1 subfamily A member 2 poor metabolizer787363003
- CYP1A2 (cytochrome P450 family 1 subfamily A member 2) rapid metaboliser787367002
- CYP1A2 (cytochrome P450 family 1 subfamily A member 2) rapid metabolizer787367002
- CYP1A2 rapid metaboliser787367002
- CYP1A2 rapid metabolizer787367002
- Cytochrome P450 family 1 subfamily A member 2 rapid metaboliser787367002
- Cytochrome P450 family 1 subfamily A member 2 rapid metabolizer787367002
- CYP1A2 (cytochrome P450 family 1 subfamily A member 2) ultra-rapid metaboliser787369004
- CYP1A2 (cytochrome P450 family 1 subfamily A member 2) ultra-rapid metabolizer787369004
- CYP1A2 ultra-rapid metaboliser787369004
- CYP1A2 ultra-rapid metabolizer787369004
- Cytochrome P450 family 1 subfamily A member 2 ultra-rapid metaboliser787369004
- Cytochrome P450 family 1 subfamily A member 2 ultra-rapid metabolizer787369004
- CYP3A4 (cytochrome P450 family 3 subfamily A member 4) poor metaboliser787380004
- CYP3A4 (cytochrome P450 family 3 subfamily A member 4) poor metabolizer787380004
- CYP3A4 poor metaboliser787380004
- CYP3A4 poor metabolizer787380004
- Cytochrome P450 family 3 subfamily A member 4 poor metaboliser787380004
- Cytochrome P450 family 3 subfamily A member 4 poor metabolizer787380004
- CYP3A4 (cytochrome P450 family 3 subfamily A member 4) rapid metaboliser787385009
- CYP3A4 (cytochrome P450 family 3 subfamily A member 4) rapid metabolizer787385009
- CYP3A4 rapid metaboliser787385009
- CYP3A4 rapid metabolizer787385009
- Cytochrome P450 family 3 subfamily A member 4 rapid metaboliser787385009
- Cytochrome P450 family 3 subfamily A member 4 rapid metabolizer787385009
- CYP3A4 (cytochrome P450 family 3 subfamily A member 4) ultra-rapid metaboliser787386005
- CYP3A4 (cytochrome P450 family 3 subfamily A member 4) ultra-rapid metabolizer787386005
- CYP3A4 ultra-rapid metaboliser787386005
- CYP3A4 ultra-rapid metabolizer787386005
- Cytochrome P450 family 3 subfamily A member 4 ultra-rapid metaboliser787386005
- Cytochrome P450 family 3 subfamily A member 4 ultra-rapid metabolizer787386005
- CYP3A5 (cytochrome P450 family 3 subfamily A member 5) ultra-rapid metaboliser787406007
- CYP3A5 (cytochrome P450 family 3 subfamily A member 5) ultra-rapid metabolizer787406007
- CYP3A5 ultra-rapid metaboliser787406007
- CYP3A5 ultra-rapid metabolizer787406007
- Cytochrome P450 family 3 subfamily A member 5 ultra-rapid metaboliser787406007
- Cytochrome P450 family 3 subfamily A member 5 ultra-rapid metabolizer787406007
- CYP2D6 (cytochrome P450 family 2 subfamily D member 6) rapid metaboliser787433006
- CYP2D6 (cytochrome P450 family 2 subfamily D member 6) rapid metabolizer787433006
- CYP2D6 rapid metaboliser787433006
- CYP2D6 rapid metabolizer787433006
- Cytochrome P450 family 2 subfamily D member 6 rapid metaboliser787433006
- Cytochrome P450 family 2 subfamily D member 6 rapid metabolizer787433006
- HPV (human papillomavirus) DNA (deoxyribonucleic acid) test positive787723002
- Human papillomavirus deoxyribonucleic acid detected787723002
- Human papillomavirus deoxyribonucleic acid test positive787723002
- Arylamine N-acetyltransferase 2 slow acetylator792857006
- N-acetyltransferase 2 slow acetylator792857006
- NAT 2 (N-acetyltransferase 2) poor metaboliser792857006
- NAT 2 (N-acetyltransferase 2) poor metabolizer792857006
- NAT2 (N-acetyltransferase 2) slow acetylator792857006
- Genetic susceptibility to malignant hyperthermia890189007
- Malignant hyperthermia genetic susceptibility890189007
- CYP4F2 (cytochrome P450 family 4 subfamily F member 2) poor metaboliser1003612008
- CYP4F2 (cytochrome P450 family 4 subfamily F member 2) poor metabolizer1003612008
- CYP4F2 poor metaboliser1003612008
- CYP4F2 poor metabolizer1003612008
- Cytochrome P450 family 4 subfamily F member 2 poor metaboliser1003612008
- Cytochrome P450 family 4 subfamily F member 2 poor metabolizer1003612008
- Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation1141749000
- Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation positive1141749000
- Malignant hyperthermia predisposition due to CACNA1S (calcium voltage-gated channel subunit alpha1 S) gene mutation positive1141749000
- Uncertain genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation1142134000
- Uncertain malignant hyperthermia predisposition due to RyR1 gene mutation1142134000
- CYP2C9 *3/*3 poor metaboliser1144910008
- CYP2C9 *3/*3 poor metabolizer1144910008
- Cytochrome P450 family 2 subfamily C member 9 *3/*3 poor metaboliser1144910008
- Cytochrome P450 family 2 subfamily C member 9 *3/*3 poor metabolizer1144910008
- CYP2C9 *2/*3 poor metaboliser1144930007
- CYP2C9 *2/*3 poor metabolizer1144930007
- Cytochrome P450 family 2 subfamily C member 9 *2/*3 poor metaboliser1144930007
- Cytochrome P450 family 2 subfamily C member 9 *2/*3 poor metabolizer1144930007
- HER2 (human epidermal growth factor receptor 2) gene amplification detected1162602001
- Human epidermal growth factor receptor 2 gene amplification detected1162602001
- Amniotic fluid alpha-fetoprotein above reference range1172710005
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome1172900005
- Amniotic fluid volume below reference range1228877003
- Finding of oligohydramnios1228877003
- Liquor volume below reference range1228877003
- CK-19 (cytokeratin-19) fragment above reference range1254667009
- CYFRA 21-1 above reference range1254667009
- Cytokeratin 19 fragment above reference range1254667009
- K19 (keratin-19) fragment above reference range1254667009
- Keratin, type I cytoskeletal 19 fragment above reference range1254667009
- High risk HPV (human papillomavirus) DNA (deoxyribonucleic acid) detected1269497006
- High risk human papillomavirus deoxyribonucleic acid detected1269497006
- High risk human papillomavirus deoxyribonucleic acid test positive1269497006
- High-risk HPV (human papillomavirus) DNA test positive1269497006
- Heterozygous NFKB inhibitor alpha gene mutation detected1279971008
- Heterozygous NFKBIA gene mutation detected1279971008
- Heterozygous NFKBIA gene mutation positive1279971008
- Heterozygous nuclear factor of kappa light polypeptide gene enhancer In B-cells inhibitor, alpha gene mutation positive1279971008
- Missense1306850007
- Missense mutation1306850007
- Splice site mutation1306851006
- Intron 1 inversion1306859008
- Inv1 - intron 1 inversion1306859008
- Intron 22 inversion1306860003
- Inv22 - intron 22 inversion1306860003
- Synonymous single nucleotide substitution1306861004
- Structural variant1331913009
- Small deletion1336122005
- Small insertion1336123000
- Mutation of promoter1336206001
- Promoter mutation1336206001
- Mutation of untranslated region1336209008
- UTR (untranslated region) mutation1336209008
- ABCG2 poor function1351232003
- ATP binding cassette subfamily G member 2 poor function1351232003
- ABCG2 decreased function1351233008
- ATP binding cassette subfamily G member 2 decreased function1351233008
- Autosomal dominant combined immunodeficiency due to STAT5b deficiency1351779004
- Autosomal dominant combined immunodeficiency due to STAT5b mutation1351779004
- Autosomal dominant combined immunodeficiency due to signal transducer and activator of transcription 5B mutation1351779004
- Autosomal recessive combined immunodeficiency due to REL mutation1351780001
- Autosomal recessive combined immunodeficiency due to REL proto-oncogene NF-kappa-B subunit mutation1351780001
- Autosomal recessive combined immunodeficiency due to c-Rel deficiency1351780001
- Autosomal recessive combined immunodeficiency due to BCL10 deficiency1351781002
- Autosomal recessive combined immunodeficiency due to BCL10 immune signaling adaptor mutation1351781002
- Autosomal recessive combined immunodeficiency due to BCL10 mutation1351781002
- Autosomal recessive combined immunodeficiency due to CHUK mutation1351800009
- Autosomal recessive combined immunodeficiency due to IKK-alpha deficiency1351800009
- Autosomal recessive combined immunodeficiency due to component of inhibitor of nuclear factor kappa B kinase complex mutation1351800009
- Combined immunodeficiency due to HELIOS deficiency1351801008
- Combined immunodeficiency due to IKAROS family zinc finger 2 mutation1351801008
- Combined immunodeficiency due to IKZF2 mutation1351801008
- Autosomal recessive combined immunodeficiency due to ITPKB deficiency1351802001
- Autosomal recessive combined immunodeficiency due to ITPKB mutation1351802001
- Autosomal recessive combined immunodeficiency due to inositol-trisphosphate 3-kinase B mutation1351802001
- Autosomal recessive combined immunodeficiency due to MAN2B2 deficiency1351946008
- Autosomal recessive combined immunodeficiency due to MAN2B2 mutation1351946008
- Autosomal recessive combined immunodeficiency due to mannosidase alpha class 2B member 2 mutation1351946008
- Oxygen saturation above reference range1351951002
- Autosomal recessive CVID (common variable immunodeficiency) due to CD20 deficiency1351960005
- Autosomal recessive common variable immunodeficiency due to CD20 deficiency1351960005
- Autosomal recessive common variable immunodeficiency due to CD20 mutation1351960005
- Autosomal recessive common variable immunodeficiency due to MS4A1 mutation1351960005
- Autosomal recessive common variable immunodeficiency due to membrane spanning 4-domains A1 mutation1351960005
- Autosomal recessive CVID (common variable immunodeficiency) due to CD21 deficiency1351961009
- Autosomal recessive common variable immunodeficiency due to CD21 deficiency1351961009
- Autosomal recessive common variable immunodeficiency due to CD21 mutation1351961009
- Autosomal recessive common variable immunodeficiency due to CR2 mutation1351961009
- Autosomal recessive common variable immunodeficiency due to complement C3d receptor 2 mutation1351961009
- Autosomal recessive CVID (combined variable immunodeficiency) due to TNFRSF13C mutation1352023006
- Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation1352023006
- Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency1352023006
- Autosomal recessive combined variable immunodeficiency due to BAFF-R deficiency1352023006
- Autosomal recessive combined variable immunodeficiency due to BAFF-R mutation1352023006
- Autosomal dominant CVID (combined variable immunodeficiency) due to TNFSF12 mutation1352026003
- Autosomal dominant combined variable immunodeficiency due to TWEAK deficiency1352026003
- Autosomal dominant combined variable immunodeficiency due to TWEAK mutation1352026003
- Autosomal dominant combined variable immunodeficiency due to tumor necrosis factor-like weak inducer of apoptosis mutation1352026003
- Autosomal dominant combined variable immunodeficiency due to tumour necrosis factor-like weak inducer of apoptosis mutation1352026003
- Autosomal dominant CVID (combined variable immunodeficiency) due to NFKB1 deficiency1354416002
- Autosomal dominant combined variable immunodeficiency due to NFKB1 deficiency1354416002
- Autosomal dominant combined variable immunodeficiency due to NFKB1 mutation1354416002
- Autosomal dominant combined variable immunodeficiency due to nuclear factor kappa B subunit 1 mutation1354416002
- Autosomal dominant CVID (combined variable immunodeficiency) due to IRF2BP2 deficiency1354420003
- Autosomal dominant combined variable immunodeficiency due to IRF2BP2 deficiency1354420003
- Autosomal dominant combined variable immunodeficiency due to IRF2BP2 mutation1354420003
- Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation1354420003
- Autosomal recessive CVID (combined variable immunodeficiency) due to ARHGEF1 deficiency1354472008
- Autosomal recessive combined variable immunodeficiency due to ARHGEF1 deficiency1354472008
- Autosomal recessive combined variable immunodeficiency due to ARHGEF1 mutation1354472008
- Autosomal recessive combined variable immunodeficiency due to Rho guanine nucleotide exchange factor 1 mutation1354472008
- Autosomal dominant CVID (combined variable immunodeficiency) due to SEC61A1 deficiency1354480001
- Autosomal dominant combined variable immunodeficiency due to SEC61 translocon subunit alpha 1 mutation1354480001
- Autosomal dominant combined variable immunodeficiency due to SEC61A1 deficiency1354480001
- Autosomal dominant combined variable immunodeficiency due to SEC61A1 mutation1354480001
- Autosomal recessive CVID (combined variable immunodeficiency) due to PIK3CG deficiency1354483004
- Autosomal recessive combined variable immunodeficiency due to PIK3CG deficiency1354483004
- Autosomal recessive combined variable immunodeficiency due to PIK3CG mutation1354483004
- Autosomal recessive combined variable immunodeficiency due to phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma mutation1354483004
- Autosomal recessive common variable immunodeficiency due to BOB1 deficiency1354596000
- Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 mutation1354596000
- Autosomal recessive common variable immunodeficiency due to POU2AF1 mutation1354596000
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome with combined immunodeficiency due to diaphanous related formin 1 mutation1354858008
- Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 deficiency1354858008
- Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 mutation1354858008
- SCBMS (seizures, cortical blindness, microcephaly syndrome) with combined immunodeficiency due to DIAPH1 mutation1354858008
- Constitutional mismatch repair deficiency syndrome due to PMS1 homolog 2, mismatch repair system component mutation1356823008
- Constitutional mismatch repair deficiency syndrome due to PMS2 deficiency1356823008
- Constitutional mismatch repair deficiency syndrome due to PMS2 mutation1356823008
- PTEN (phosphatase and tensin homolog) gene mutation detected1357792009
- Phosphatase and tensin homolog gene mutation detected1357792009
- CYP2C9 *5/*6 poor metaboliser1363066005
- CYP2C9 *5/*6 poor metabolizer1363066005
- Cytochrome P450 family 2 subfamily C member 9 *5/*6 poor metaboliser1363066005
- Cytochrome P450 family 2 subfamily C member 9 *5/*6 poor metabolizer1363066005
- CYP2C9 *6/*6 poor metaboliser1363067001
- CYP2C9 *6/*6 poor metabolizer1363067001
- Cytochrome P450 family 2 subfamily C member 9 *6/*6 poor metaboliser1363067001
- Cytochrome P450 family 2 subfamily C member 9 *6/*6 poor metabolizer1363067001
- CYP2C9 *6/*8 poor metaboliser1363069003
- CYP2C9 *6/*8 poor metabolizer1363069003
- Cytochrome P450 family 2 subfamily C member 9 *6/*8 poor metaboliser1363069003
- Cytochrome P450 family 2 subfamily C member 9 *6/*8 poor metabolizer1363069003
- CYP2C9 *6/*11 poor metaboliser1363070002
- CYP2C9 *6/*11 poor metabolizer1363070002
- Cytochrome P450 family 2 subfamily C member 9 *6/*11 poor metaboliser1363070002
- Cytochrome P450 family 2 subfamily C member 9 *6/*11 poor metabolizer1363070002
- Lynch syndrome gene mutation detected1365861003
- High risk variant of APOL1 (apolipoprotein L1) gene detected1365952004
- High risk variant of apolipoprotein L1 gene detected1365952004
- Low risk variant of APOL1 (apolipoprotein L1) gene detected1365954003
- Low risk variant of apolipoprotein L1 gene detected1365954003
- B-Raf serine/threonine kinase gene mutation detected961321000124101
- BRAF serine threonine kinase gene mutation detected961321000124101
- BRAF serine threonine kinase gene mutation positive961321000124101
- Down syndrome detected by multiple marker screening130081000119101
- Multiple marker screen positive for Down syndrome130081000119101
- Multiple marker screening test positive for Down syndrome130081000119101
- Triple screening test positive for Down syndrome130081000119101
- Genetic susceptibility to cancer85121000119109
- Genetic susceptibility to genetic disorder71951000119107
- High risk HPV (human papillomavirus) test positive97401000146106
- High risk human papillomavirus detected97401000146106
- High risk human papillomavirus positive97401000146106
- Increased nuchal translucency detected by multiple marker screening286571000119101
- Multiple marker screen positive for increased nuchal translucency286571000119101
- Multiple marker screen positive for trisomy 18130071000119104
- Trisomy 18 detected by multiple marker screening130071000119104
- Triplicated alpha globin gene689861000119100
- Triplication of alpha globin gene689861000119100
Frequently Asked Questions
What is ICD-10 code R89.8?
ICD-10-CM code R89.8 represents "Other abnormal findings in specimens from other organs, systems and tissues". It is a billable/specific code that can be used on a claim.
Is R89.8 a billable code?
Yes, R89.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is R89.8 in?
R89.8 is in Chapter 18: Symptoms, Signs and Abnormal Clinical and Laboratory Findings (codes R00-R99).
What codes cannot be used with R89.8?
R89.8 has Excludes1 notes indicating codes that cannot be used together with it, including: abnormal findings on antenatal screening of mother (O28.-); diagnostic abnormal findings classified elsewhere - see Alphabetical Index.
What SNOMED CT codes does R89.8 map to?
R89.8 maps to 331 SNOMED CT concepts: 1351233008, 1351232003, 166561008, 69604007, 42170009, and 326 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for R89.8?
R89.8 is linked to 2 UMLS Concept Unique Identifiers: C2830575, C0478185. 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.