Index to Diseases and Injuries
Deficiency, deficient
- 3-beta hydroxysteroid dehydrogenase E25.0
- 5-alpha reductase (with male pseudohermaphroditism) E29.1
- 11-hydroxylase E25.0
- 21-hydroxylase E25.0
- AADC (aromatic L-amino acid decarboxylase) E70.81
- ABCC6 →
- abdominal muscle syndrome Q79.4
- accelerator globulin (Ac G) (blood) D68.2
- AC globulin (congenital) (hereditary) →
- acid phosphatase E83.39
- acid sphingomyelinase (ASMD) →
- activating factor (blood) D68.2
- ADA2 (adenosine deaminase 2) D81.32
- adenosine deaminase (ADA) →
- aldolase (hereditary) E74.19
- alpha-1-antitrypsin E88.01
- amino-acids E72.9
- anemia — see Anemia
- aneurin E51.9
- antibody with →
- antidiuretic hormone E23.2
- anti-hemophilic →
- antithrombin (antithrombin III) D68.59
- aromatic L-amino acid decarboxylase (AADC) E70.81
- ascorbic acid E54
- attention (disorder) (syndrome) →
- autoprothrombin →
- beta-glucuronidase E76.29
- biotin E53.8
- biotin-dependent carboxylase D81.819
- biotinidase D81.810
- brancher enzyme (amylopectinosis) E74.03
- calciferol →
- calcium (dietary) E58
- calorie, severe →
- cardiac — see Insufficiency, myocardial
- carnitine →
- carotene E50.9
- CD73 deficiency causing arterial calcification E83.825
- central nervous system G96.89
- ceruloplasmin (Wilson) E83.01
- choline E53.8
- Christmas factor D67
- chromium E61.4
- chronic neurovisceral acid sphingomyelinase E75.244
- chronic visceral acid sphingomyelinase E75.241
- clotting (blood) D68.9 — see also Deficiency, coagulation factor
- clotting factor NEC (hereditary) D68.2 — see also Deficiency, factor
- coagulation NOS →
- cognitive F09
- color vision →
- combined glucocorticoid and mineralocorticoid E27.49
- contact factor D68.2
- copper (nutritional) E61.0
- corticoadrenal →
- craniofacial axis Q75.009
- cyanocobalamin E53.8
- C1 esterase inhibitor (C1-INH) D84.1
- debrancher enzyme (limit dextrinosis) E74.03
- dehydrogenase →
- diet E63.9
- dihydropyrimidine dehydrogenase (DPD) E88.89
- disaccharidase E73.9
- edema — see Malnutrition, severe
- endocrine E34.9
- energy-supply — see Malnutrition
- ENPP1 →
- enzymes, circulating NEC E88.09
- ergosterol →
- essential fatty acid (EFA) E63.0
- eye movements →
- factor →
- femoral, proximal focal (congenital) — see Defect, reduction, lower limb, longitudinal, femur
- fibrin-stabilizing factor (congenital) (hereditary) →
- fibrinase D68.2
- fibrinogen (congenital) (hereditary) →
- folate E53.8
- folic acid E53.8
- foreskin N47.3
- fructokinase E74.11
- fructose 1,6-diphosphatase E74.19
- fructose-1-phosphate aldolase E74.19
- GABA (gamma aminobutyric acid) transaminase E72.81
- GABA-T (gamma aminobutyric acid transaminase) E72.81
- GABA transporter 1 QA0.0131
- galactokinase E74.29
- galactose-1-phosphate uridyl transferase E74.29
- gammaglobulin in blood →
- glass factor D68.2
- glucocorticoid →
- glucose-6-phosphatase E74.01
- glucose-6-phosphate dehydrogenase →
- glucose transporter protein type 1 E74.810
- glucuronyl transferase E80.5
- Glut1 E74.810
- glycogen synthetase E74.09
- gonadotropin (isolated) E23.0
- growth hormone (idiopathic) (isolated) E23.0
- Hageman factor D68.2
- hemoglobin D64.9
- hepatophosphorylase E74.09
- homogentisate 1,2-dioxygenase E70.29
- hormone →
- hypoxanthine- (guanine)-phosphoribosyltransferase (HG- PRT) (total H-PRT) E79.1
- immunity →
- immuno — see Immunodeficiency
- immunoglobulin, selective →
- infantile neurovisceral acid sphingomyelinase E75.240
- inositol (B complex) E53.8
- intrinsic →
- iodine →
- iron →
- kalium E87.6
- kappa-light chain D80.8
- labile factor (congenital) (hereditary) →
- lacrimal fluid (acquired) →
- lactase →
- Laki-Lorand factor D68.2
- LCAD (long chain acyl CoA dehydrogenase deficiency) E71.310
- lecithin cholesterol acyltransferase E78.6
- leukocyte adhesion (LAD-I) (LAD-II) (LAD-III) →
- lipocaic K86.89
- lipoprotein (familial) (high density) E78.6
- liver phosphorylase E74.09
- lysosomal alpha-1, 4 glucosidase E74.02
- lysosome-associated membrane protein 2 [LAMP2] E74.05
- magnesium E61.2
- major histocompatibility complex →
- manganese E61.3
- MCAD (medium chain acyl CoA dehydrogenase deficiency) E71.311
- menadione (vitamin K) →
- mental (familial) (hereditary) — see Disability, intellectual
- methylenetetrahydrofolate reductase (MTHFR) E72.12
- mevalonate kinase M04.1
- mineral NEC E61.8
- mineralocorticoid →
- molybdenum (nutritional) E61.5
- moral F60.2
- multiple nutrient elements E61.7
- multiple sulfatase (MSD) E75.26
- muscle →
- myoadenylate deaminase E79.2
- myocardial — see Insufficiency, myocardial
- myophosphorylase E74.04
- NADH diaphorase or reductase (congenital) D74.0
- NADH-methemoglobin reductase (congenital) D74.0
- natrium E87.1
- niacin (amide) (-tryptophan) E52
- nicotinamide E52
- nicotinic acid E52
- number of teeth — see Anodontia
- nutrient element →
- nutrition, nutritional →
- of interleukin 1 receptor antagonist [DIRA] M04.8
- ornithine transcarbamylase E72.4
- ovarian E28.39
- oxygen — see Anoxia
- pantothenic acid E53.8
- parathyroid (gland) E20.9
- perineum (female) N81.89
- phenylalanine hydroxylase E70.1
- phosphoenolpyruvate carboxykinase E74.4
- phosphofructokinase E74.19
- phosphomannomutase E74.818
- phosphomannose isomerase E74.818
- phosphomannosyl mutase E74.818
- phosphorylase kinase, liver E74.09
- pituitary hormone (isolated) E23.0
- plasma thromboplastin →
- plasminogen (type 1) (type 2) E88.02
- platelet NEC →
- polyglandular →
- potassium (K) E87.6
- prepuce N47.3
- proaccelerin (congenital) (hereditary) →
- proconvertin factor (congenital) (hereditary) →
- protein →
- prothrombin (congenital) (heredItary) →
- Prower factor D68.2
- pseudocholinesterase E88.09
- PTA (plasma thromboplastin antecedent) D68.1
- PTC (plasma thromboplastin component) D67
- purine nucleoside phosphorylase (PNP) D81.5
- pyracin (alpha) (beta) E53.1
- pyridoxal E53.1
- pyridoxamine E53.1
- pyridoxine (derivatives) E53.1
- pyruvate →
- riboflavin (vitamin B2) E53.0
- salt E87.1
- SCAD (short chain acyl CoA dehydrogenase deficiency) E71.312
- secretion →
- selenium (dietary) E59
- serum antitrypsin, familial E88.01
- short stature homeobox gene (SHOX) →
- sodium (Na) E87.1
- SPCA (factor VII) D68.2
- sphincter, intrinsic →
- stable factor (congenital) (hereditary) →
- Stuart-Prower (factor X) D68.2
- succinic semialdehyde dehydrogenase E72.81
- sucrase E74.39
- sulfatase E75.26
- sulfite oxidase E72.19
- thiamin, thiaminic (chloride) →
- thrombokinase →
- thyroid (gland) — see Hypothyroidism
- tocopherol E56.0
- tooth bud K00.0
- transcobalamine II (anemia) D51.2
- vanadium E61.6
- vascular I99.9
- vasopressin E23.2
- vertical ridge K06.8
- viosterol — see Deficiency, calciferol
- vitamin (multiple) NOS →
- VLCAD (very long chain acyl CoA dehydrogenase deficiency) E71.310
- von Willebrand factor →
- zinc, dietary E60
Use the index to find a code, then confirm it in the Tabular List before assigning it. A code ending in a dash is incomplete, and a code in [brackets] is a manifestation code reported after the underlying condition. Search the whole index.
ICD-10-CM Index to Diseases and Injuries maintained by CDC/NCHS (public domain), from the CMS FY2027 release.