Bone marrow erythropoiesis hyperplasia
Galactose below reference range
Molecular dissociation
Increase of specific gravity
Influenza A virus subtype H1 detected
Constitutional mismatch repair deficiency syndrome due to PMS1 homolog 2, mismatch repair system component mutation
CYP2C9 *3/*3 poor metabolizer
Hardening
Calculus chemical composition - finding
Acellular smear
Abnormally hard consistency
Autosomal dominant combined variable immunodeficiency due to NFKB1 deficiency
CYP2C9 ultra-rapid metaboliser
Increased glucose level
Cytochrome P450 family 1 subfamily A member 2 poor metabolizer
Calculus = bilirubin
Deoxyribonucleic acid damage
Macromolecular defective synthesis
DNA damage
Synovial fluid viscosity - finding
Laxness
Intron 22 inversion
Finding by inspection (simple observation)
Uroporphyrin below reference range
Cytochrome P450 family 2 subfamily C member 9 *3/*3 poor metaboliser
Genetic mutation
ABCG2 poor function
Presence of crystals
Constitutional mismatch repair deficiency syndrome due to PMS2 mutation
Protein conformation
Abnormal presence of glucose
Abnormally increased laxity
VKORC1 (vitamin K epoxide reductase complex 1) poor metaboliser
Malignant hyperthermia predisposition due to CACNA1S (calcium voltage-gated channel subunit alpha1 S) gene mutation positive
CYP3A4 (cytochrome P450 family 3 subfamily A member 4) poor metabolizer
Autosomal recessive common variable immunodeficiency due to membrane spanning 4-domains A1 mutation
Abnormal organ weight
Increased macromolecular binding
Arylamine N-acetyltransferase 2 slow acetylator
Vitamin K epoxide reductase complex 1 ultra-rapid metabolizer
Decreased orotic acid
Genetic linkage disequilibrium
Abnormal size
Tyrosine below reference range
HER2 (human epidermal growth factor receptor 2) gene amplification detected
Autosomal dominant combined immunodeficiency due to STAT5b deficiency
Autosomal recessive combined immunodeficiency due to MAN2B2 mutation
Needle shaped crystals present
CYP4F2 (cytochrome P450 family 4 subfamily F member 2) poor metaboliser
Specimen grossly icteric
Protein electrophoresis abnormal
Specific gravity above reference range
Joint fluid turbid
Synovial fluid: crystals
Autosomal dominant combined variable immunodeficiency due to SEC61A1 mutation
Finding of vitamin B12 level
GU test observation
Nucleic acid conformation
Genetic susceptibility to cancer
Carbohydrate conformation
Increased translucency
CYP2C9 *2/*3 poor metaboliser
B-Raf serine/threonine kinase gene mutation detected
Cancer antigen 27-29 above reference range
Genetic mosaic
Inv1 - intron 1 inversion
Mannoheptulose above reference range
Urobilin below reference range
Autosomal recessive common variable immunodeficiency due to complement C3d receptor 2 mutation
Autosomal recessive combined variable immunodeficiency due to ARHGEF1 deficiency
VKORC1 ultra-rapid metabolizer
Finding of specific gravity
Decreased galactose
Abnormal chromosomal findings in specimens from other organs, systems and tissues
Human papillomavirus deoxyribonucleic acid detected
Abnormal nucleic acid sequence
Cytochrome P450 family 2 subfamily C member 9 *6/*8 poor metaboliser
CYP2C9 (cytochrome P450 family 2 subfamily C member 9) ultra-rapid metabolizer
Increased glycogen
CYP3A5 (cytochrome P450 family 3 subfamily A member 5) ultra-rapid metaboliser
CYP1A2 poor metabolizer
Increased methemalbumin
Specimen slightly icteric
ABCG2 decreased function
Autosomal recessive combined variable immunodeficiency due to BAFF-R mutation
Joint fluid yellow
Presence of ova cysts and parasites
Tumor protein p53 detected
Molecular inactivation
Synovial fluid: abnormal content
Specimen hemolyzed
Amino acid below reference range
Monocyte count - finding
CYP2C9 ultra-rapid metabolizer
Decreased methemalbumin
Cytochrome P450 family 3 subfamily A member 5 ultra-rapid metaboliser
Decreased porphyrin
Abnormal presence of hemoglobin
Methaemalbumin below reference range
Amniotic fluid alpha-fetoprotein abnormal
Carbohydrate above reference range
Pentose above reference range
CYP2C9 *6/*11 poor metabolizer
CYP3A4 (cytochrome P450 family 3 subfamily A member 4) poor metaboliser
Autosomal dominant combined variable immunodeficiency due to TWEAK mutation
Cytochrome P450 family 1 subfamily A member 2 rapid metabolizer
Histidine below reference range
BRAF serine threonine kinase gene mutation positive
Amniotic fluid AFP - finding
Cytochrome P450 family 4 subfamily F member 2 poor metaboliser
Ascorbic acid below reference range
Increased xanthine
Vitamin B below reference range
SCBMS (seizures, cortical blindness, microcephaly syndrome) with combined immunodeficiency due to DIAPH1 mutation
Cell division alteration
Vitamin D above reference range
Increased fructose
CYP3A5 ultra-rapid metaboliser
Increased laxity
Adenylic acid below reference range
Genetic finding detected
CYP1A2 (cytochrome P450 family 1 subfamily A member 2) poor metaboliser
Combined immunodeficiency due to IKAROS family zinc finger 2 mutation
Bone marrow megaloblastic
Mitotic arrest
Biliverdin above reference range
Heterozygous NFKBIA gene mutation detected
Combined immunodeficiency due to HELIOS deficiency
Calculus = hydroxyapatite
Decreased amino acid
Increased lactic acid level
CYP2C9 *3/*3 poor metaboliser
Increased galactose
Breast cancer genetic marker of susceptibility detected
Abnormal presence of protein
CYP3A4 rapid metaboliser
Abnormal nucleotide base sequence
Decreased ceroid
Finding of quantity of amniotic fluid
Mucopurulent
Specimen grossly lipaemic
Trisomy 18 detected by multiple marker screening
Abnormal macromolecular binding
Suture material present
Observation of quantity of liquor
Increased ketone bodies
CYP2C9 poor metabolizer
Heterozygous protocadherin 19 gene mutation detected
VKORC1 (vitamin K epoxide reductase complex 1) rapid metabolizer
NAT 2 (N-acetyltransferase 2) poor metabolizer
Alteration of genetic material
Autosomal recessive CVID (combined variable immunodeficiency) due to TNFRSF13C mutation
Autosomal recessive combined variable immunodeficiency due to PIK3CG mutation
Abnormally increased organ weight
Missense
Snowstorm knee
Small insertion
Malignant hyperthermia genetic susceptibility
CYP2C9 *5/*6 poor metaboliser
Protein-bound iodine below reference range
DNA injury
Amniotic fluid abnormal
Mitochondrial 1555 A to G mutation detected
Cytochrome P450 family 2 subfamily C member 9 *3/*3 poor metabolizer
Decreased molecular dissociation
Cortical blindness
Decreased lactose
Suppressor mutation
Constitutional mismatch repair deficiency syndrome due to PMS2 deficiency
Small deletion
Gene re-arrangement, B lymphocyte
Sample hemolyzed
Fibrinogen below reference range
Urobilin above reference range
Quantity of liquor
Sample slightly lipaemic
Abnormal carbohydrate sequence
Synovial fluid turbid
Inequality in circumference
Genetic susceptibility to genetic disorder
Pentose below reference range
Gene re-arrangement, T lymphocyte
Autosomal dominant combined variable immunodeficiency due to nuclear factor kappa B subunit 1 mutation
Decreased vitamin C
Porphyrin below reference range
Decreased size
Finding of amniotic fluid alpha-fetoprotein
Specimen lipemic
Glycogen above reference range
CYP4F2 poor metaboliser
Increased urobilin
Increased vitamin K
Vitamin B12 above reference range
Synovial fluid viscosity low
Decreased glycogen
Abnormal bone marrow iron
Multiple marker screen positive for increased nuchal translucency
CYP1A2 (cytochrome P450 family 1 subfamily A member 2) poor metabolizer
Specific gravity
Uric acid level below reference range
Cytochrome P450 family 3 subfamily A member 4 ultra-rapid metabolizer
Granulopenia
Increased ascorbic acid
Homogentisic acid above reference range
Autosomal recessive common variable immunodeficiency due to POU2AF1 mutation
Abnormal presence of galactose
Translucency finding
CYP2C9 rapid metaboliser
Cytochrome P450 family 2 subfamily C member 9 *6/*8 poor metabolizer
Amniotic fluid AFP
High risk human papillomavirus deoxyribonucleic acid test positive
Calculus = phosphate
Cytochrome P450 family 3 subfamily A member 4 rapid metabolizer
Xanthine below reference range
Abnormal amniotic fluid
Decrease in circumference
Decreased translucency
Lynch syndrome gene mutation detected
Amniotic fluid alpha-fetoprotein above reference range
Finding of contact sensitivity response
Frame-shift mutation
Finding of synovial fluid viscosity
Cytochrome P450 family 1 subfamily A member 2 poor metaboliser
CYP1A2 poor metaboliser
Increased amino acid
Mitotic alteration
Specimen haemolysed
CYP1A2 (cytochrome P450 family 1 subfamily A member 2) ultra-rapid metabolizer
Sample slightly icteric
Decreased bilirubin level
CYP1A2 ultra-rapid metaboliser
CYP2C9 *6/*11 poor metaboliser
Abnormal structure of physiologic substance
Increased molecular dissociation
Histidine above reference range
Uncertain malignant hyperthermia predisposition due to RyR1 gene mutation
Autosomal recessive CVID (common variable immunodeficiency) due to CD21 deficiency
Globulin below reference range
High risk variant of apolipoprotein L1 gene detected
Vitamin K epoxide reductase complex 1 ultra-rapid metaboliser
CK-19 (cytokeratin-19) fragment above reference range
Macromolecular cleavage
Cell chromosome examination abnormal
Multiple marker screen positive for Down syndrome
Cystine above reference range
Calculus = carbaptite
Cytochrome P450 family 2 subfamily C member 9 poor metaboliser
Cytochrome P450 family 2 subfamily C member 9 *5/*6 poor metaboliser
Molecular degradation
Gene re-arrangement
Specimen grossly lipemic
Cytochrome P450 family 3 subfamily A member 4 poor metabolizer
Gene amplification
Synovial fluid cloudy
Vanillylmandelic acid level below reference range
Beta amino isobutyric acid above reference range
Decreased vanillylmandelic acid level
Amino acid above reference range
Cold agglutinins present
Methaemalbumin above reference range
Decreased tyrosine
Choline above reference range
Calculus chemical composition
Autosomal dominant CVID (combined variable immunodeficiency) due to IRF2BP2 deficiency
Heterozygous NFKB inhibitor alpha gene mutation detected
CYP3A4 ultra-rapid metabolizer
Synovial fluid: uric acid
Amniotic fluid alpha-fetoprotein outside reference range
Increased adenylic acid
Decreased carbohydrate
Finding of synovial fluid composition
Cytochrome P450 family 4 subfamily F member 2 poor metabolizer
Synovial fluid viscosity high
Autosomal recessive combined variable immunodeficiency due to Rho guanine nucleotide exchange factor 1 mutation
Autosomal dominant combined variable immunodeficiency due to SEC61A1 deficiency
CYP2C9 rapid metabolizer
CYFRA 21-1 above reference range
Finding of oxygen saturation
Cytochrome P450 family 1 subfamily A member 2 ultra-rapid metaboliser
Uncertain genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation
Contact sensitivity response - finding
Methemalbumin above reference range
Increased cystine
Promoter mutation
Triplication of alpha globin gene
Monocyte count outside reference range
Low risk variant of APOL1 (apolipoprotein L1) gene detected
Vitamin B12 level
Autosomal recessive combined immunodeficiency due to mannosidase alpha class 2B member 2 mutation
Cytochrome P450 family 2 subfamily C member 9 rapid metaboliser
CYP2C9 *6/*8 poor metabolizer
Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 deficiency
Satisfactory for evaluation but limited by partially obscuring air drying artifact
Increased pentose
High risk human papillomavirus detected
Specimen slightly hemolyzed
Autosomal recessive common variable immunodeficiency due to CD20 deficiency
Autosomal dominant combined immunodeficiency due to signal transducer and activator of transcription 5B mutation
Decreased urobilin
Glycogen below reference range
Abnormal quantity of physiologic substance
CYP2D6 (cytochrome P450 family 2 subfamily D member 6) rapid metaboliser
Increased cell mitotic activity
Sample lipemic
Gene re-arrangement, B lymphocyte, light chain
Cystine below reference range
Thyroid hormone level below reference range
Autosomal recessive combined immunodeficiency due to BCL10 mutation
Abnormal structure of cerebroside
Autosomal recessive combined immunodeficiency due to MAN2B2 deficiency
Inv22 - intron 22 inversion
Missense mutation
Gene re-arrangement, gamma chain, T cell antigen receptor
Allelic exclusion
Multiple marker screen positive for trisomy 18
Autosomal recessive combined immunodeficiency due to REL proto-oncogene NF-kappa-B subunit mutation
Increased homogentisic acid
Autosomal recessive common variable immunodeficiency due to CD20 mutation
Specific gravity - finding
Sample grossly icteric
CYP2C9 *6/*6 poor metabolizer
Structural variant
Influenza A H1N1 virus 2009 pandemic strain present
GU test finding
Autosomal dominant combined variable immunodeficiency due to IRF2BP2 mutation
Increased histidine
Ketone bodies above reference range
Constitutional mismatch repair deficiency syndrome
Decreased protein-bound iodine
Urobilinogen level below reference range
NAT2 (N-acetyltransferase 2) slow acetylator
Folic acid above reference range
Autosomal recessive combined immunodeficiency due to REL mutation
Satisfactory for evaluation but limited by partially obscuring thick areas
Autosomal recessive common variable immunodeficiency due to CD21 mutation
Heterozygous protocadherin 19 gene mutation positive
VKORC1 poor metaboliser
Vesicular reaction
Phosphate calculus of kidney
Cytochrome P450 family 2 subfamily C member 19 rapid metaboliser
Heterozygous nuclear factor of kappa light polypeptide gene enhancer In B-cells inhibitor, alpha gene mutation positive
High risk HPV (human papillomavirus) DNA (deoxyribonucleic acid) detected
Phosphatase and tensin homolog gene mutation detected
UTR (untranslated region) mutation
Autosomal recessive combined immunodeficiency due to component of inhibitor of nuclear factor kappa B kinase complex mutation
CYP1A2 ultra-rapid metabolizer
Cytochrome P450 family 2 subfamily C member 9 ultra-rapid metabolizer
N-acetyltransferase 2 slow acetylator
Specimen involvement by multifocal invasion
Karyotype evaluation abnormal
VKORC1 ultra-rapid metaboliser
Autosomal recessive combined immunodeficiency due to ITPKB mutation
Decreased fibrinogen
Depolymerization
Finding of presence of crystals
Increased methaemalbumin
Increased vanillylmandelic acid level
Increased vitamin A
Macromolecular nicking
Mutation of promoter
Sample grossly hemolyzed
Macromolecular binding
Autosomal recessive combined variable immunodeficiency due to PIK3CG deficiency
Decreased uroporphyrin
Finding of amniotic fluid volume
Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation
Synovial fluid: pyrophosphate
CYP3A5 (cytochrome P450 family 3 subfamily A member 5) ultra-rapid metabolizer
Protein electrophoresis outside reference range
CYP3A4 (cytochrome P450 family 3 subfamily A member 4) ultra-rapid metaboliser
Decreased cystine
Sample grossly lipemic
Abnormal macromolecular sequence
CMMR-D (constitutional mismatch repair deficiency) syndrome
Orotic acid above reference range
Autosomal recessive CVID (common variable immunodeficiency) due to CD20 deficiency
Vitamin K epoxide reductase complex 1 poor metaboliser
Shrinkage
Effect of antioestrogen agent
Amniotic fluid AFP (alpha-fetoprotein) abnormal
Mutation of untranslated region
VKORC1 (vitamin K epoxide reductase complex 1) poor metabolizer
Specimen lipaemic
Fructose below reference range
Mannoheptulose below reference range
Mitochondrial 1555 A to G mutation positive
Lactose above reference range
Cytochrome P450 family 2 subfamily C member 9 *2/*3 poor metabolizer
Folic acid below reference range
Heterozygous NFKBIA gene mutation positive
Nonsense mutation
Alpha-fetoprotein above reference range
Carbohydrate below reference range
Oxygen saturation above reference range
Autosomal dominant combined immunodeficiency due to STAT5b mutation
Molecular conformation
Multiple marker screening test positive for Down syndrome
CYP3A4 rapid metabolizer
Synovial fluid bloodstained
Autosomal recessive combined immunodeficiency due to BCL10 deficiency
Calculus = triple phosphate
Cytochrome P450 family 2 subfamily C member 9 *6/*11 poor metabolizer
CYP2D6 rapid metabolizer
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome
Orotic acid below reference range
Fructose above reference range
Joint fluid hemorrhagic
Positive genetic finding
CYP2C9 (cytochrome P450 family 2 subfamily C member 9) rapid metabolizer
Abnormal presence of myoglobin
Tyrosine above reference range
Finding of bone marrow erythropoiesis
Positive for tumor protein p53
CYP3A5 ultra-rapid metabolizer
Autosomal recessive combined variable immunodeficiency due to phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma mutation
CYP1A2 rapid metabolizer
Autosomal recessive common variable immunodeficiency due to BOB1 deficiency
CYP2C9 *6/*6 poor metaboliser
VKORC1 rapid metabolizer
Cytochrome P450 family 2 subfamily C member 9 poor metabolizer
Increased mannoheptulose
Molecular instability
Conformational change
Decreased beta amino isobutyric acid
ATP binding cassette subfamily G member 2 decreased function
Autosomal dominant CVID (combined variable immunodeficiency) due to TNFSF12 mutation
NAT 2 (N-acetyltransferase 2) poor metaboliser
Phosphate kidney stone
Methemalbumin below reference range
Specimen slightly lipemic
Vitamin K epoxide reductase complex 1 rapid metabolizer
CYP1A2 rapid metaboliser
Denaturation
High risk HPV (human papillomavirus) test positive
Sample lipaemic
Influenza A virus subtype H1 present
Addition-deletion mutation
CYP2C9 poor metaboliser
Cytochrome P450 family 2 subfamily C member 19 rapid metabolizer
Triplicated alpha globin gene
Ascorbic acid above reference range
Specimen slightly haemolysed
CYP2D6 rapid metaboliser
Intron 1 inversion
Beta amino isobutyric acid below reference range
Cytochrome P450 family 2 subfamily C member 9 *2/*3 poor metaboliser
Autosomal recessive combined immunodeficiency due to c-Rel deficiency
Decreased adenosine monophosphate
Foetal tissue present in specimen
Decreased histidine
Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency
Galactose above reference range
Cytokeratin 19 fragment above reference range
Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 mutation
Breast cancer genetic marker of susceptibility positive
Abnormal presence of pentose
CYP2C9 (cytochrome P450 family 2 subfamily C member 9) ultra-rapid metaboliser
CYP4F2 (cytochrome P450 family 4 subfamily F member 2) poor metabolizer
Finding of presence of ova cysts and parasites
VKORC1 (vitamin K epoxide reductase complex 1) ultra-rapid metaboliser
Cytochrome P450 family 2 subfamily C member 9 *6/*6 poor metabolizer
Cytochrome P450 family 2 subfamily D member 6 rapid metabolizer
Human papillomavirus deoxyribonucleic acid test positive
Increased ceroid
Synovial fluid: fibrin clot +
Joint fluid haemorrhagic
High cancer antigen 27-29 level
Autosomal dominant CVID (combined variable immunodeficiency) due to NFKB1 deficiency
Abnormal presence of haemoglobin
Measurement finding below reference range
Autosomal recessive combined immunodeficiency due to IKK-alpha deficiency
Rarefaction
Abnormally soft consistency
Presence of crystals - finding
Down syndrome detected by multiple marker screening
Adenylic acid above reference range
Unstable molecule
Tumour protein p53 detected
Increase in circumference
VKORC1 (vitamin K epoxide reductase complex 1) ultra-rapid metabolizer
Abnormal thickness
Lactose below reference range
Decreased globulin
Autosomal dominant combined variable immunodeficiency due to SEC61 translocon subunit alpha 1 mutation
Decreased cell mitotic activity
Decreased pentose
Autosomal dominant combined variable immunodeficiency due to TWEAK deficiency
CYP2C19 rapid metaboliser
CYP3A4 ultra-rapid metaboliser
Cytochrome P450 family 1 subfamily A member 2 rapid metaboliser
Stringing of synovial fluid
Finding of monocyte count
Macromolecular alteration
Cytochrome P450 family 3 subfamily A member 5 ultra-rapid metabolizer
Bone marrow normoblastic
Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation
Increased orotic acid
Vitamin E above reference range
Combined immunodeficiency due to IKZF2 mutation
Autosomal recessive common variable immunodeficiency due to CD21 deficiency
Increased carbohydrate
Increased adenosine monophosphate
Fetal tissue present in specimen
Joint fluid bloody
VKORC1 rapid metaboliser
Synovial fluid composition - finding
Vitamin K epoxide reductase complex 1 poor metabolizer
Autosomal recessive common variable immunodeficiency due to MS4A1 mutation
Blood in synovial fluid
K19 (keratin-19) fragment above reference range
Cholesterol/high density lipoprotein ratio above reference range
Lactic acid level above reference range
Increased beta amino isobutyric acid
Sample slightly lipemic
Autosomal recessive combined variable immunodeficiency due to BAFF-R deficiency
Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 mutation
Specimen icteric
Vitamin A above reference range
Abnormal molecular cross-linking
Tissue specimen fragmented
Cytochrome P450 family 2 subfamily D member 6 rapid metaboliser
Measurement finding above reference range
Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation positive
Decreased xanthine
Synonymous single nucleotide substitution
Finding of oligohydramnios
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome with combined immunodeficiency due to diaphanous related formin 1 mutation
Decreased urobilinogen level
High-risk HPV (human papillomavirus) DNA test positive
Cytochrome P450 family 3 subfamily A member 4 rapid metaboliser
Decreased choline
Synovial fluid yellow
Decreased ascorbic acid
Abnormal amino acid sequence
Cytochrome P450 family 3 subfamily A member 4 poor metaboliser
Foetal anomaly present in specimen
Increased vitamin D
Extra chromosomal inheritance
CYP2C9 *5/*6 poor metabolizer
Finding related to physiologic substance
Choline below reference range
Autosomal dominant CVID (combined variable immunodeficiency) due to SEC61A1 deficiency
Decreased thyroid hormone level
Depolymerisation
Specimen slightly lipaemic
Positive for tumour protein p53
Bone marrow iron finding
ATP binding cassette subfamily G member 2 poor function
Abnormal structure of phospholipid
Decreased methaemalbumin
Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation
CYP3A4 (cytochrome P450 family 3 subfamily A member 4) ultra-rapid metabolizer
Superhelicity
Cytochrome P450 family 2 subfamily C member 9 *5/*6 poor metabolizer
Mutation of p53 gene
Abnormally increased laxness
Laxity
CYP3A4 poor metaboliser
Cytochrome P450 family 3 subfamily A member 4 ultra-rapid metaboliser
Decreased mannoheptulose
CYP3A4 (cytochrome P450 family 3 subfamily A member 4) rapid metabolizer
Somatic mutation
Genetic susceptibility to malignant hyperthermia
Mutation of p53 gene present
Genetic variation
Autosomal recessive combined immunodeficiency due to CHUK mutation
BRAF serine threonine kinase gene mutation detected
Temperature-sensitive mutation
Increased folic acid
VKORC1 poor metabolizer
Autosomal recessive combined immunodeficiency due to ITPKB deficiency
Decreased folic acid
Sample grossly lipaemic
CYP2D6 (cytochrome P450 family 2 subfamily D member 6) rapid metabolizer
Calculus = cholesterol
VKORC1 (vitamin K epoxide reductase complex 1) rapid metaboliser
Specimen too thick for optimal interpretation
Specimen grossly hemolyzed
Genitourinary test finding
Point mutation
Absent bone marrow iron
Glucose level above reference range
HPV (human papillomavirus) DNA (deoxyribonucleic acid) test positive
Cytochrome P450 family 1 subfamily A member 2 ultra-rapid metabolizer
Cytochrome P450 family 2 subfamily C member 9 *6/*11 poor metaboliser
Decreased fructose
Increased laxness
Autosomal dominant combined variable immunodeficiency due to IRF2BP2 deficiency
Decreased macromolecular binding
Genetic linkage equilibrium
Gene re-arrangement, alpha chain, T cell antigen receptor
CYP1A2 (cytochrome P450 family 1 subfamily A member 2) rapid metaboliser
Abnormal consistency
Decreased uric acid level
Increased urobilinogen level
Vitamin K epoxide reductase complex 1 rapid metaboliser
Alpha-fetoprotein raised
Gene re-arrangement, beta chain, T cell antigen receptor
Triple screening test positive for Down syndrome
Effect of antiestrogen agent
Amount of liquor
Monocyte count abnormal
Finding of synovial fluid appearance
Mitochondrial mutation
Diminution of size
Sample slightly haemolysed
Retraction
Aceto-white reaction finding
Meiotic alteration
High risk variant of APOL1 (apolipoprotein L1) gene detected
Finding of calculus chemical composition
Increased vitamin B12
Sample grossly haemolysed
Urobilinogen level above reference range
Finding of bilirubin level
High risk human papillomavirus deoxyribonucleic acid detected
Autosomal recessive common variable immunodeficiency due to CR2 mutation
CYP2C19 rapid metabolizer
Keratin, type I cytoskeletal 19 fragment above reference range
Autosomal recessive CVID (combined variable immunodeficiency) due to PIK3CG deficiency
Cytochrome P450 family 2 subfamily C member 9 ultra-rapid metaboliser
Genetic inversion
Autosomal dominant combined variable immunodeficiency due to tumour necrosis factor-like weak inducer of apoptosis mutation
Autosomal dominant combined variable immunodeficiency due to NFKB1 mutation
Autosomal dominant combined variable immunodeficiency due to tumor necrosis factor-like weak inducer of apoptosis mutation
Abnormal translucency
Defective molecular assembly
Human epidermal growth factor receptor 2 gene amplification detected
Low risk variant of apolipoprotein L1 gene detected
Decreased vitamin B
Abnormally decreased organ weight
CYP1A2 (cytochrome P450 family 1 subfamily A member 2) rapid metabolizer
Elevated cholesterol/high density lipoprotein ratio
CYP3A4 poor metabolizer
Strand breaks
Decreased adenylic acid
Increased tyrosine
Increased lactose
Sample slightly hemolyzed
Satisfactory for evaluation but limited by partially obscuring air drying artefact
Increased biliverdin
Increased vitamin E
Finding of quantity of liquor
Increased vitamin C
Positive skin test reaction
PTEN (phosphatase and tensin homolog) gene mutation detected
Splice site mutation
Monocyte count
Finding of organ weight
Bilirubin level - finding
CYP1A2 (cytochrome P450 family 1 subfamily A member 2) ultra-rapid metaboliser
Vitamin K above reference range
Cytochrome P450 family 2 subfamily C member 9 rapid metabolizer
Aceto-white reaction positive
Synovial fluid fibrin clot
Gene re-arrangement, B lymphocyte, heavy chain
Liquor volume below reference range
CYP4F2 poor metabolizer
Autosomal recessive CVID (combined variable immunodeficiency) due to ARHGEF1 deficiency
Increased diameter
Amniotic fluid volume below reference range
Quantity of physiologic substance outside reference range
Vanillylmandelic acid level above reference range
CYP2C9 *2/*3 poor metabolizer
Xanthine above reference range
High risk human papillomavirus positive
AFP - Alpha-fetoprotein raised
Autosomal recessive combined variable immunodeficiency due to ARHGEF1 mutation
Joint fluid cloudy
Nucleotide base deletion
Sample haemolysed
Bilirubin level below reference range
Bilirubin level
Smear too thick for optimal interpretation
Cold agglutinins detected
Fetal anomaly present in specimen
Sample icteric
CYP2C9 *6/*8 poor metaboliser
Increased choline
Granulocyte count below reference range
Increased nuchal translucency detected by multiple marker screening
Presence of ova cysts and parasites - finding
Reading-frame-shift mutation
Autosomal recessive combined immunodeficiency due to BCL10 immune signaling adaptor mutation
Autosomal recessive combined immunodeficiency due to inositol-trisphosphate 3-kinase B mutation
CYP2C9 (cytochrome P450 family 2 subfamily C member 9) rapid metaboliser
Specimen grossly haemolysed
Tissue specimen ruptured
Cytochrome P450 family 2 subfamily C member 9 *6/*6 poor metaboliser
Fragmented tissue specimen
CYP3A4 (cytochrome P450 family 3 subfamily A member 4) rapid metaboliser

Frequently Asked Questions

What is the ICD-10 code for oth abnormal findings in specimens from oth org/tiss?

The ICD-10-CM code for oth abnormal findings in specimens from oth org/tiss is R89.8. The full clinical description is "Other abnormal findings in specimens from other organs, systems and tissues". R89.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code R89.8 mean?

ICD-10-CM code R89.8 represents “Other abnormal findings in specimens from other organs, systems and tissues”. It is classified under Chapter 18: Symptoms, Signs and Abnormal Clinical and Laboratory Findings and 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.

How does R89.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth abnormal findings in specimens from oth org/tiss affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of R89.8?

R89.8 maps to the ICD-11 code: MG6Y (Other specified clinical findings in specimens from other specified organs, systems and tissues).

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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.