ICD-10-CM Alphabetic Index
Deficiency, deficient
Sub-terms(219)
—ABCC6—AC globulin(congenital) (hereditary)D68.2—acid sphingomyelinase(ASMD)E75.249—adenosine deaminase(ADA)D81.30—antibody with—anti-hemophilic—attention(disorder) (syndrome)F98.8—autoprothrombin—calciferolE55.9—calorie, severeE43—carnitineE71.40—coagulation NOSD68.9—color visionH53.50—corticoadrenalE27.40—dehydrogenase—ENPP1—ergosterolE55.9—eye movements—factor—fibrin-stabilizing factor(congenital) (hereditary)D68.2—fibrinogen(congenital) (hereditary)D68.2—gammaglobulin in bloodD80.1—glucocorticoidE27.49—glucose-6-phosphate dehydrogenase—hormone—immunityD84.9—immunoglobulin, selective—intrinsic—iodineE61.8—ironE61.1—labile factor(congenital) (hereditary)D68.2—lacrimal fluid(acquired)—lactase—leukocyte adhesion(LAD-I) (LAD-II) (LAD-III)D71.1—major histocompatibility complex—menadione(vitamin K)E56.1—mineralocorticoidE27.49—muscle—nutrient elementE61.9—nutrition, nutritionalE63.9—plasma thromboplastin—platelet NECD69.1—polyglandularE31.8—proaccelerin(congenital) (hereditary)D68.2—proconvertin factor(congenital) (hereditary)D68.2—proteinE46—prothrombin(congenital) (heredItary)D68.2—pyruvate—secretion—short stature homeobox gene(SHOX)—sphincter, intrinsicN36.42—stable factor(congenital) (hereditary)D68.2—thiamin, thiaminic(chloride)E51.9—thrombokinaseD68.2—vitamin NOS(multiple)E56.9—von Willebrand factor—3-beta hydroxysteroid dehydrogenaseE25.0—5-alpha reductase(with male pseudohermaphroditism)E29.1—11-hydroxylaseE25.0—21-hydroxylaseE25.0—AADC(aromatic L-amino acid decarboxylase)E70.81—abdominal muscle syndromeQ79.4—accelerator globulin(Ac G) (blood)D68.2—acid phosphataseE83.39—activating factor(blood)D68.2—ADA2(adenosine deaminase 2)D81.32—aldolase(hereditary)E74.19—alpha-1-antitrypsinE88.01—amino-acidsE72.9—aneurinE51.9—antidiuretic hormoneE23.2—antithrombin(antithrombin III)D68.59—aromatic L-amino acid decarboxylase(AADC)E70.81—ascorbic acidE54—beta-glucuronidaseE76.29—biotinE53.8—biotin-dependent carboxylaseD81.819—biotinidaseD81.810—brancher enzyme(amylopectinosis)E74.03—calcium(dietary)E58—caroteneE50.9—CD73 deficiency causing arterial calcificationE83.825—central nervous systemG96.89—ceruloplasmin(Wilson)E83.01—cholineE53.8—Christmas factorD67—chromiumE61.4—chronic neurovisceral acid sphingomyelinaseE75.244—chronic visceral acid sphingomyelinaseE75.241—clotting(blood)D68.9—clotting factor NEC(hereditary)D68.2—cognitiveF09—combined glucocorticoid and mineralocorticoidE27.49—contact factorD68.2—copper(nutritional)E61.0—craniofacial axisQ75.009—cyanocobalaminE53.8—C1 esterase inhibitor(C1-INH)D84.1—debrancher enzyme(limit dextrinosis)E74.03—dietE63.9—dihydropyrimidine dehydrogenase(DPD)E88.89—disaccharidaseE73.9—endocrineE34.9—enzymes, circulating NECE88.09—essential fatty acid(EFA)E63.0—fibrinaseD68.2—folateE53.8—folic acidE53.8—foreskinN47.3—fructokinaseE74.11—fructose 1,6-diphosphataseE74.19—fructose-1-phosphate aldolaseE74.19—GABA transaminase(gamma aminobutyric acid)E72.81—GABA-T(gamma aminobutyric acid transaminase)E72.81—GABA transporter 1QA0.0131—galactokinaseE74.29—galactose-1-phosphate uridyl transferaseE74.29—glass factorD68.2—glucose-6-phosphataseE74.01—glucose transporter protein type 1E74.810—glucuronyl transferaseE80.5—Glut1E74.810—glycogen synthetaseE74.09—gonadotropin(isolated)E23.0—growth hormone(idiopathic) (isolated)E23.0—Hageman factorD68.2—hemoglobinD64.9—hepatophosphorylaseE74.09—homogentisate 1,2-dioxygenaseE70.29—hypoxanthine-(guanine)-phosphoribosyltransferase (HG- PRT) (total H-PRT)E79.1—infantile neurovisceral acid sphingomyelinaseE75.240—inositol(B complex)E53.8—kaliumE87.6—kappa-light chainD80.8—Laki-Lorand factorD68.2—LCAD(long chain acyl CoA dehydrogenase deficiency)E71.310—lecithin cholesterol acyltransferaseE78.6—lipocaicK86.89—lipoprotein(familial) (high density)E78.6—liver phosphorylaseE74.09—lysosomal alpha-1, 4 glucosidaseE74.02—lysosome-associated membrane protein 2 [LAMP2]E74.05—magnesiumE61.2—manganeseE61.3—MCAD(medium chain acyl CoA dehydrogenase deficiency)E71.311—methylenetetrahydrofolate reductase(MTHFR)E72.12—mevalonate kinaseM04.1—mineral NECE61.8—molybdenum(nutritional)E61.5—moralF60.2—multiple nutrient elementsE61.7—multiple sulfatase(MSD)E75.26—myoadenylate deaminaseE79.2—myophosphorylaseE74.04—NADH diaphorase or reductase(congenital)D74.0—NADH-methemoglobin reductase(congenital)D74.0—natriumE87.1—niacin(amide) (-tryptophan)E52—nicotinamideE52—nicotinic acidE52—of interleukin 1 receptor antagonist [DIRA]M04.8—ornithine transcarbamylaseE72.4—ovarianE28.39—pantothenic acidE53.8—parathyroid(gland)E20.9—perineum(female)N81.89—phenylalanine hydroxylaseE70.1—phosphoenolpyruvate carboxykinaseE74.4—phosphofructokinaseE74.19—phosphomannomutaseE74.818—phosphomannose isomeraseE74.818—phosphomannosyl mutaseE74.818—phosphorylase kinase, liverE74.09—pituitary hormone(isolated)E23.0—plasminogen(type 1) (type 2)E88.02—potassium(K)E87.6—prepuceN47.3—Prower factorD68.2—pseudocholinesteraseE88.09—PTA(plasma thromboplastin antecedent)D68.1—PTC(plasma thromboplastin component)D67—purine nucleoside phosphorylase(PNP)D81.5—pyracin(alpha) (beta)E53.1—pyridoxalE53.1—pyridoxamineE53.1—pyridoxine(derivatives)E53.1—riboflavin(vitamin B2)E53.0—saltE87.1—SCAD(short chain acyl CoA dehydrogenase deficiency)E71.312—selenium(dietary)E59—serum antitrypsin, familialE88.01—sodium(Na)E87.1—SPCA(factor VII)D68.2—Stuart-Prower(factor X)D68.2—succinic semialdehyde dehydrogenaseE72.81—sucraseE74.39—sulfataseE75.26—sulfite oxidaseE72.19—tocopherolE56.0—tooth budK00.0—transcobalamine II(anemia)D51.2—vanadiumE61.6—vascularI99.9—vasopressinE23.2—vertical ridgeK06.8—VLCAD(very long chain acyl CoA dehydrogenase deficiency)E71.310—zinc, dietaryE60—anemiasee Anemia—cardiacsee Insufficiency, myocardial—edemasee Malnutrition, severe—energy-supplysee Malnutrition—femoral, proximal focal(congenital)see Defect, reduction, lower limb, longitudinal, femur—immunosee Immunodeficiency—mental(familial) (hereditary)see Disability, intellectual—myocardialsee Insufficiency, myocardial—number of teethsee Anodontia—oxygensee Anoxia—thyroid(gland)see Hypothyroidism—viosterolsee Deficiency, calciferol