ICD-10-CM Alphabetic Index to Diseases and Injuries
Deficiency, deficient
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- 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
- causing generalized arterial calcification of infancy E83.823
- pseudoxanthoma elasticum E83.824
- abdominal muscle syndrome Q79.4
- accelerator globulin (Ac G) (blood) D68.2
- AC globulin (congenital) (hereditary) D68.2
- acquired D68.4
- acid phosphatase E83.39
- acid sphingomyelinase (ASMD) E75.249
- type
- A E75.240
- A/B E75.244
- B E75.241
- activating factor (blood) D68.2
- ADA2 (adenosine deaminase 2) D81.32
- adenosine deaminase (ADA) D81.30
- with severe combined immunodeficiency (SCID) D81.31
- partial (type 1) D81.39
- specified NEC D81.39
- type 1 (without SCID) (without severe combined immunodeficiency) D81.39
- type 2 D81.32
- aldolase (hereditary) E74.19
- alpha-1-antitrypsin E88.01
- amino-acids E72.9
- anemia — see Anemia
- aneurin E51.9
- antibody with
- hyperimmunoglobulinemia D80.6
- near-normal immunoglobins D80.6
- antidiuretic hormone E23.2
- anti-hemophilic
- factor (A) D66
- B D67
- C D68.1
- globulin (AHG) NEC D66
- antithrombin (antithrombin III) D68.59
- aromatic L-amino acid decarboxylase (AADC) E70.81
- ascorbic acid E54
- attention (disorder) (syndrome) F98.8
- with hyperactivity — see Disorder, attention-deficit hyperactivity
- autoprothrombin
- I D68.2
- II D67
- C D68.2
- beta-glucuronidase E76.29
- biotin E53.8
- biotin-dependent carboxylase D81.819
- biotinidase D81.810
- brancher enzyme (amylopectinosis) E74.03
- calciferol E55.9
- with
- adult osteomalacia M83.8
- rickets — see Rickets
- calcium (dietary) E58
- calorie, severe E43
- with marasmus E41
- and kwashiorkor E42
- cardiac — see Insufficiency, myocardial
- carnitine E71.40
- due to
- hemodialysis E71.43
- inborn errors of metabolism E71.42
- Valproic acid therapy E71.43
- iatrogenic E71.43
- muscle palmityltransferase E71.314
- primary E71.41
- secondary E71.448
- 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 D68.9
- with
- ectopic pregnancy O08.1
- molar pregnancy O08.1
- acquired (any) D68.4
- antepartum hemorrhage — see Hemorrhage, antepartum, with coagulation defect
- clotting factor NEC D68.2 — see also Deficiency, factor
- due to
- hyperprothrombinemia D68.4
- liver disease D68.4
- vitamin K deficiency D68.4
- newborn, transient P61.6
- postpartum O72.3
- specified NEC D68.8
- cognitive F09
- color vision H53.50
- achromatopsia H53.51
- acquired H53.52
- deuteranomaly H53.53
- protanomaly H53.54
- specified type NEC H53.59
- tritanomaly H53.55
- combined glucocorticoid and mineralocorticoid E27.49
- contact factor D68.2
- copper (nutritional) E61.0
- corticoadrenal E27.40
- primary E27.1
- craniofacial axis Q75.009
- cyanocobalamin E53.8
- C1 esterase inhibitor (C1-INH) D84.1
- debrancher enzyme (limit dextrinosis) E74.03
- dehydrogenase
- long chain/very long chain acyl CoA E71.310
- medium chain acyl CoA E71.311
- short chain acyl CoA E71.312
- diet E63.9
- dihydropyrimidine dehydrogenase (DPD) E88.89
- disaccharidase E73.9
- edema — see Malnutrition, severe
- endocrine E34.9
- energy-supply — see Malnutrition
- ENPP1
- causing
- autosomal recessive hypophosphatemic rickets type 2 E83.822
- generalized arterial calcification of infancy E83.821
- enzymes, circulating NEC E88.09
- ergosterol E55.9
- with
- adult osteomalacia M83.8
- rickets — see Rickets
- essential fatty acid (EFA) E63.0
- eye movements
- saccadic H55.81
- smooth pursuit H55.82
- factor — see also Deficiency, coagulation
- Hageman D68.2
- I (congenital) (hereditary) D68.2
- II (congenital) (hereditary) D68.2
- IX (congenital) (functional) (hereditary) (with functional defect) D67
- multiple (congenital) D68.8
- acquired D68.4
- V (congenital) (hereditary) D68.2
- VII (congenital) (hereditary) D68.2
- VIII (congenital) (functional) (hereditary) (with functional defect) D66
- with vascular defect — see Disease, von Willebrand
- X (congenital) (hereditary) D68.2
- XI (congenital) (hereditary) D68.1
- XII (congenital) (hereditary) D68.2
- XIII (congenital) (hereditary) D68.2
- femoral, proximal focal (congenital) — see Defect, reduction, lower limb, longitudinal, femur
- fibrin-stabilizing factor (congenital) (hereditary) D68.2
- acquired D68.4
- fibrinase D68.2
- fibrinogen (congenital) (hereditary) D68.2
- acquired D65
- 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 D80.1
- hereditary D80.0
- glass factor D68.2
- glucocorticoid E27.49
- mineralocorticoid E27.49
- glucose-6-phosphatase E74.01
- glucose-6-phosphate dehydrogenase
- anemia D55.0
- without anemia D75.A
- 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
- anterior pituitary (partial) NEC E23.0
- growth E23.0
- growth (isolated) E23.0
- pituitary E23.0
- testicular E29.1
- hypoxanthine- (guanine)-phosphoribosyltransferase (HG- PRT) (total H-PRT) E79.1
- immunity D84.9
- cell-mediated D84.89
- with thrombocytopenia and eczema D82.0
- combined D81.9
- humoral D80.9
- IgA (secretory) D80.2
- IgG D80.3
- IgM D80.4
- immuno — see Immunodeficiency
- immunoglobulin, selective
- A (IgA) D80.2
- G (IgG) (subclasses) D80.3
- M (IgM) D80.4
- infantile neurovisceral acid sphingomyelinase E75.240
- inositol (B complex) E53.8
- intrinsic
- factor (congenital) D51.0
- sphincter N36.42
- with urethral hypermobility N36.43
- iodine E61.8
- congenital syndrome — see Syndrome, iodine-deficiency, congenital
- iron E61.1
- anemia D50.9
- kalium E87.6
- kappa-light chain D80.8
- labile factor (congenital) (hereditary) D68.2
- acquired D68.4
- lacrimal fluid (acquired) — see also Syndrome, dry eye
- congenital Q10.6
- lactase
- congenital E73.0
- secondary E73.1
- 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) D71.1
- type I D71.1
- type II D71.1
- type III D71.1
- 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
- class I D81.6
- class II D81.7
- manganese E61.3
- MCAD (medium chain acyl CoA dehydrogenase deficiency) E71.311
- menadione (vitamin K) E56.1
- newborn P53
- mental (familial) (hereditary) — see Disability, intellectual
- methylenetetrahydrofolate reductase (MTHFR) E72.12
- mevalonate kinase M04.1
- mineral NEC E61.8
- mineralocorticoid E27.49
- with glucocorticoid E27.49
- molybdenum (nutritional) E61.5
- moral F60.2
- multiple nutrient elements E61.7
- multiple sulfatase (MSD) E75.26
- muscle
- carnitine (palmityltransferase) E71.314
- phosphofructokinase E74.09
- 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 E61.9
- multiple E61.7
- specified NEC E61.8
- nutrition, nutritional E63.9 — see also Nutrition deficient
- sequelae — see Sequelae, nutritional deficiency
- specified NEC E63.8
- 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
- antecedent (PTA) D68.1
- component (PTC) D67
- plasminogen (type 1) (type 2) E88.02
- platelet NEC D69.19
- constitutional — see Disease, von Willebrand
- polyglandular E31.8
- autoimmune E31.0
- potassium (K) E87.6
- prepuce N47.3
- proaccelerin (congenital) (hereditary) D68.2
- acquired D68.4
- proconvertin factor (congenital) (hereditary) D68.2
- acquired D68.4
- protein E46 — see also Malnutrition
- anemia D53.0
- C D68.59
- S D68.59
- prothrombin (congenital) (heredItary) D68.2
- acquired D68.4
- 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
- carboxylase E74.4
- dehydrogenase E74.4
- riboflavin (vitamin B2) E53.0
- salt E87.1
- SCAD (short chain acyl CoA dehydrogenase deficiency) E71.312
- secretion
- ovary E28.39
- salivary gland (any) K11.7
- urine R34
- selenium (dietary) E59
- serum antitrypsin, familial E88.01
- short stature homeobox gene (SHOX)
- with
- dyschondrosteosis Q78.8
- short stature (idiopathic) E34.328
- Turner's syndrome Q96.9
- sodium (Na) E87.1
- SPCA (factor VII) D68.2
- sphincter, intrinsic N36.42
- with urethral hypermobility N36.43
- stable factor (congenital) (hereditary) D68.2
- acquired D68.4
- Stuart-Prower (factor X) D68.2
- succinic semialdehyde dehydrogenase E72.81
- sucrase E74.39
- sulfatase E75.26
- sulfite oxidase E72.19
- thiamin, thiaminic (chloride) E51.9
- beriberi (dry) E51.11
- wet E51.12
- thrombokinase D68.2
- newborn P53
- 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 E56.9
- A E50.9
- with
- Bitot's spot (corneal) E50.1
- follicular keratosis E50.8
- keratomalacia E50.4
- manifestations NEC E50.8
- night blindness E50.5
- scar of cornea, xerophthalmic E50.6
- xeroderma E50.8
- xerophthalmia E50.7
- xerosis
- conjunctival E50.0
- and Bitot's spot E50.1
- cornea E50.2
- and ulceration E50.3
- sequelae E64.1
- B (complex) NOS E53.9
- with
- beriberi (dry) E51.11
- wet E51.12
- pellagra E52
- B1 NOS E51.9
- beriberi (dry) E51.11
- with circulatory system manifestations E51.11
- wet E51.12
- B12 E53.8
- B2 (riboflavin) E53.0
- B6 E53.1
- C E54
- sequelae E64.2
- D E55.9
- with
- adult osteomalacia M83.8
- rickets — see Rickets
- 25-hydroxylase E83.32
- E E56.0
- folic acid E53.8
- G E53.0
- group B E53.9
- specified NEC E53.8
- H (biotin) E53.8
- K E56.1
- of newborn P53
- nicotinic E52
- P E56.8
- PP (pellagra-preventing) E52
- specified NEC E56.8
- thiamin E51.9
- beriberi — see Beriberi
- VLCAD (very long chain acyl CoA dehydrogenase deficiency) E71.310
- von Willebrand factor
- partial quantitative D68.01 — see also Disease, von Willebrand
- total quantitative D68.03 — see also Disease, von Willebrand
- zinc, dietary E60