ICD-10 code for deficiency

• 3-beta hydroxysteroid dehydrogenase E25.0 — Congenital adrenogenital disorders associated with enzyme deficiency
• 5-alpha reductase (with male pseudohermaphroditism) E29.1 — Testicular hypofunction
• 11-hydroxylase E25.0 — Congenital adrenogenital disorders associated with enzyme deficiency
• 21-hydroxylase E25.0 — Congenital adrenogenital disorders associated with enzyme deficiency
• AADC (aromatic L-amino acid decarboxylase) E70.81 — Aromatic L-amino acid decarboxylase deficiency
• ABCC6
• causing generalized arterial calcification of infancy E83.823 — ABCC6 deficiency causing generalized arterial calcification of infancy
• pseudoxanthoma elasticum E83.824 — ABCC6 deficiency causing pseudoxanthoma elasticum
• abdominal muscle syndrome Q79.4 — Prune belly syndrome
• accelerator globulin (Ac G) (blood) D68.2 — Hereditary deficiency of other clotting factors
• AC globulin (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• acquired D68.4 — Acquired coagulation factor deficiency
• acid phosphatase E83.39 — Other disorders of phosphorus metabolism
• acid sphingomyelinase (ASMD) E75.249 — Niemann-Pick disease, unspecified
• type
• A E75.240 — Niemann-Pick disease type A
• A/B E75.244 — Niemann-Pick disease type A/B
• B E75.241 — Niemann-Pick disease type B
• activating factor (blood) D68.2 — Hereditary deficiency of other clotting factors
• ADA2 (adenosine deaminase 2) D81.32 — Adenosine deaminase 2 deficiency
• adenosine deaminase (ADA) D81.30 — Adenosine deaminase deficiency, unspecified
• with severe combined immunodeficiency (SCID) D81.31 — Severe combined immunodeficiency due to adenosine deaminase deficiency
• partial (type 1) D81.39 — Other adenosine deaminase deficiency
• specified NEC D81.39 — Other adenosine deaminase deficiency
• type 1 (without SCID) (without severe combined immunodeficiency) D81.39 — Other adenosine deaminase deficiency
• type 2 D81.32 — Adenosine deaminase 2 deficiency
• aldolase (hereditary) E74.19 — Other disorders of fructose metabolism
• alpha-1-antitrypsin E88.01 — Alpha-1-antitrypsin deficiency
• amino-acids E72.9 — Disorder of amino-acid metabolism, unspecified
• anemia
• aneurin E51.9 — Thiamine deficiency, unspecified
• antibody with
• hyperimmunoglobulinemia D80.6 — Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
• near-normal immunoglobins D80.6 — Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
• antidiuretic hormone E23.2 — Diabetes insipidus
• anti-hemophilic
• factor (A) D66 — Hereditary factor VIII deficiency
• B D67 — Hereditary factor IX deficiency
• C D68.1 — Hereditary factor XI deficiency
• globulin (AHG) NEC D66 — Hereditary factor VIII deficiency
• antithrombin (antithrombin III) D68.59 — Other primary thrombophilia
• aromatic L-amino acid decarboxylase (AADC) E70.81 — Aromatic L-amino acid decarboxylase deficiency
• ascorbic acid E54 — Ascorbic acid deficiency
• attention (disorder) (syndrome) F98.8 — Other specified behavioral and emotional disorders with onset usually occurring in childhood and adolescence
• with hyperactivity
• autoprothrombin
• I D68.2 — Hereditary deficiency of other clotting factors
• II D67 — Hereditary factor IX deficiency
• C D68.2 — Hereditary deficiency of other clotting factors
• beta-glucuronidase E76.29 — Other mucopolysaccharidoses
• biotin E53.8 — Deficiency of other specified B group vitamins
• biotin-dependent carboxylase D81.819 — Biotin-dependent carboxylase deficiency, unspecified
• biotinidase D81.810 — Biotinidase deficiency
• brancher enzyme (amylopectinosis) E74.03 — Cori disease
• calciferol E55.9 — Vitamin D deficiency, unspecified
• with
• adult osteomalacia M83.8 — Other adult osteomalacia
• rickets
• calcium (dietary) E58 — Dietary calcium deficiency
• calorie, severe E43 — Unspecified severe protein-calorie malnutrition
• with marasmus E41 — Nutritional marasmus
• and kwashiorkor E42 — Marasmic kwashiorkor
• cardiac
• carnitine E71.40 — Disorder of carnitine metabolism, unspecified
• due to
• hemodialysis E71.43 — Iatrogenic carnitine deficiency
• inborn errors of metabolism E71.42 — Carnitine deficiency due to inborn errors of metabolism
• Valproic acid therapy E71.43 — Iatrogenic carnitine deficiency
• iatrogenic E71.43 — Iatrogenic carnitine deficiency
• muscle palmityltransferase E71.314 — Muscle carnitine palmitoyltransferase deficiency
• primary E71.41 — Primary carnitine deficiency
• secondary E71.448 — Other secondary carnitine deficiency
• carotene E50.9 — Vitamin A deficiency, unspecified
• CD73 deficiency causing arterial calcification E83.825 — CD73 deficiency causing arterial calcification
• central nervous system G96.89 — Other specified disorders of central nervous system
• ceruloplasmin (Wilson) E83.01 — Wilson's disease
• choline E53.8 — Deficiency of other specified B group vitamins
• Christmas factor D67 — Hereditary factor IX deficiency
• chromium E61.4 — Chromium deficiency
• chronic neurovisceral acid sphingomyelinase E75.244 — Niemann-Pick disease type A/B
• chronic visceral acid sphingomyelinase E75.241 — Niemann-Pick disease type B
• clotting (blood) D68.9 — Coagulation defect, unspecified
• clotting factor NEC (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• coagulation NOS D68.9 — Coagulation defect, unspecified
• with
• ectopic pregnancy O08.1 — Delayed or excessive hemorrhage following ectopic and molar pregnancy
• molar pregnancy O08.1 — Delayed or excessive hemorrhage following ectopic and molar pregnancy
• acquired (any) D68.4 — Acquired coagulation factor deficiency
• antepartum hemorrhage
• clotting factor NEC D68.2 — Hereditary deficiency of other clotting factors
• due to
• hyperprothrombinemia D68.4 — Acquired coagulation factor deficiency
• liver disease D68.4 — Acquired coagulation factor deficiency
• vitamin K deficiency D68.4 — Acquired coagulation factor deficiency
• newborn, transient P61.6 — Other transient neonatal disorders of coagulation
• postpartum O72.3 — Postpartum coagulation defects
• specified NEC D68.8 — Other specified coagulation defects
• cognitive F09 — Unspecified mental disorder due to known physiological condition
• color vision H53.50 — Unspecified color vision deficiencies
• achromatopsia H53.51 — Achromatopsia
• acquired H53.52 — Acquired color vision deficiency
• deuteranomaly H53.53 — Deuteranomaly
• protanomaly H53.54 — Protanomaly
• specified type NEC H53.59 — Other color vision deficiencies
• tritanomaly H53.55 — Tritanomaly
• combined glucocorticoid and mineralocorticoid E27.49 — Other adrenocortical insufficiency
• contact factor D68.2 — Hereditary deficiency of other clotting factors
• copper (nutritional) E61.0 — Copper deficiency
• corticoadrenal E27.40 — Unspecified adrenocortical insufficiency
• primary E27.1 — Primary adrenocortical insufficiency
• craniofacial axis Q75.009 — Craniosynostosis, unspecified
• cyanocobalamin E53.8 — Deficiency of other specified B group vitamins
• C1 esterase inhibitor (C1-INH) D84.1 — Defects in the complement system
• debrancher enzyme (limit dextrinosis) E74.03 — Cori disease
• dehydrogenase
• long chain/very long chain acyl CoA E71.310 — Long chain/very long chain acyl CoA dehydrogenase deficiency
• medium chain acyl CoA E71.311 — Medium chain acyl CoA dehydrogenase deficiency
• short chain acyl CoA E71.312 — Short chain acyl CoA dehydrogenase deficiency
• diet E63.9 — Nutritional deficiency, unspecified
• dihydropyrimidine dehydrogenase (DPD) E88.89 — Other specified metabolic disorders
• disaccharidase E73.9 — Lactose intolerance, unspecified
• edema
• endocrine E34.9 — Endocrine disorder, unspecified
• energy-supply
• ENPP1
• causing
• autosomal recessive hypophosphatemic rickets type 2 E83.822 — ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
• generalized arterial calcification of infancy E83.821 — ENPP1 deficiency causing generalized arterial calcification of infancy
• enzymes, circulating NEC E88.09 — Other disorders of plasma-protein metabolism, not elsewhere classified
• ergosterol E55.9 — Vitamin D deficiency, unspecified
• with
• adult osteomalacia M83.8 — Other adult osteomalacia
• rickets
• essential fatty acid (EFA) E63.0 — Essential fatty acid [EFA] deficiency
• eye movements
• saccadic H55.81 — Deficient saccadic eye movements
• smooth pursuit H55.82 — Deficient smooth pursuit eye movements
• factor
• Hageman D68.2 — Hereditary deficiency of other clotting factors
• I (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• II (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• IX (congenital) (functional) (hereditary) (with functional defect) D67 — Hereditary factor IX deficiency
• multiple (congenital) D68.8 — Other specified coagulation defects
• acquired D68.4 — Acquired coagulation factor deficiency
• V (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• VII (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• VIII (congenital) (functional) (hereditary) (with functional defect) D66 — Hereditary factor VIII deficiency
• with vascular defect
• X (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• XI (congenital) (hereditary) D68.1 — Hereditary factor XI deficiency
• XII (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• XIII (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• femoral, proximal focal (congenital)
• fibrin-stabilizing factor (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• acquired D68.4 — Acquired coagulation factor deficiency
• fibrinase D68.2 — Hereditary deficiency of other clotting factors
• fibrinogen (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• acquired D65 — Disseminated intravascular coagulation [defibrination syndrome]
• folate E53.8 — Deficiency of other specified B group vitamins
• folic acid E53.8 — Deficiency of other specified B group vitamins
• foreskin N47.3 — Deficient foreskin
• fructokinase E74.11 — Essential fructosuria
• fructose 1,6-diphosphatase E74.19 — Other disorders of fructose metabolism
• fructose-1-phosphate aldolase E74.19 — Other disorders of fructose metabolism
• GABA (gamma aminobutyric acid) transaminase E72.81 — Disorders of gamma aminobutyric acid metabolism
• GABA-T (gamma aminobutyric acid transaminase) E72.81 — Disorders of gamma aminobutyric acid metabolism
• GABA transporter 1 QA0.0131 — SLC6A1-related disorder
• galactokinase E74.29 — Other disorders of galactose metabolism
• galactose-1-phosphate uridyl transferase E74.29 — Other disorders of galactose metabolism
• gammaglobulin in blood D80.1 — Nonfamilial hypogammaglobulinemia
• hereditary D80.0 — Hereditary hypogammaglobulinemia
• glass factor D68.2 — Hereditary deficiency of other clotting factors
• glucocorticoid E27.49 — Other adrenocortical insufficiency
• mineralocorticoid E27.49 — Other adrenocortical insufficiency
• glucose-6-phosphatase E74.01 — von Gierke disease
• glucose-6-phosphate dehydrogenase
• anemia D55.0 — Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
• without anemia D75.A — Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
• glucose transporter protein type 1 E74.810 — Glucose transporter protein type 1 deficiency
• glucuronyl transferase E80.5 — Crigler-Najjar syndrome
• Glut1 E74.810 — Glucose transporter protein type 1 deficiency
• glycogen synthetase E74.09 — Other glycogen storage disease
• gonadotropin (isolated) E23.0 — Hypopituitarism
• growth hormone (idiopathic) (isolated) E23.0 — Hypopituitarism
• Hageman factor D68.2 — Hereditary deficiency of other clotting factors
• hemoglobin D64.9 — Anemia, unspecified
• hepatophosphorylase E74.09 — Other glycogen storage disease
• homogentisate 1,2-dioxygenase E70.29 — Other disorders of tyrosine metabolism
• hormone
• anterior pituitary (partial) NEC E23.0 — Hypopituitarism
• growth E23.0 — Hypopituitarism
• growth (isolated) E23.0 — Hypopituitarism
• pituitary E23.0 — Hypopituitarism
• testicular E29.1 — Testicular hypofunction
• hypoxanthine- (guanine)-phosphoribosyltransferase (HG- PRT) (total H-PRT) E79.1 — Lesch-Nyhan syndrome
• immunity D84.9 — Immunodeficiency, unspecified
• cell-mediated D84.89 — Other immunodeficiencies
• with thrombocytopenia and eczema D82.0 — Wiskott-Aldrich syndrome
• combined D81.9 — Combined immunodeficiency, unspecified
• humoral D80.9 — Immunodeficiency with predominantly antibody defects, unspecified
• IgA (secretory) D80.2 — Selective deficiency of immunoglobulin A [IgA]
• IgG D80.3 — Selective deficiency of immunoglobulin G [IgG] subclasses
• IgM D80.4 — Selective deficiency of immunoglobulin M [IgM]
• immuno
• immunoglobulin, selective
• A (IgA) D80.2 — Selective deficiency of immunoglobulin A [IgA]
• G (IgG) (subclasses) D80.3 — Selective deficiency of immunoglobulin G [IgG] subclasses
• M (IgM) D80.4 — Selective deficiency of immunoglobulin M [IgM]
• infantile neurovisceral acid sphingomyelinase E75.240 — Niemann-Pick disease type A
• inositol (B complex) E53.8 — Deficiency of other specified B group vitamins
• intrinsic
• factor (congenital) D51.0 — Vitamin B12 deficiency anemia due to intrinsic factor deficiency
• sphincter N36.42 — Intrinsic sphincter deficiency (ISD)
• with urethral hypermobility N36.43 — Combined hypermobility of urethra and intrinsic sphincter deficiency
• iodine E61.8 — Deficiency of other specified nutrient elements
• congenital syndrome
• iron E61.1 — Iron deficiency
• anemia D50.9 — Iron deficiency anemia, unspecified
• kalium E87.6 — Hypokalemia
• kappa-light chain D80.8 — Other immunodeficiencies with predominantly antibody defects
• labile factor (congenital) (hereditary) D68.2 — Hereditary deficiency of other clotting factors
• acquired D68.4 — Acquired coagulation factor deficiency
• lacrimal fluid (acquired)
• congenital Q10.6 — Other congenital malformations of lacrimal apparatus
• lactase
• congenital E73.0 — Congenital lactase deficiency
• secondary E73.1 — Secondary lactase deficiency
• Laki-Lorand factor D68.2 — Hereditary deficiency of other clotting factors
• LCAD (long chain acyl CoA dehydrogenase deficiency) E71.310 — Long chain/very long chain acyl CoA dehydrogenase deficiency
• lecithin cholesterol acyltransferase E78.6 — Lipoprotein deficiency
• leukocyte adhesion (LAD-I) (LAD-II) (LAD-III) D71.1 — Leukocyte adhesion deficiency
• type I D71.1 — Leukocyte adhesion deficiency
• type II D71.1 — Leukocyte adhesion deficiency
• type III D71.1 — Leukocyte adhesion deficiency
• lipocaic K86.89 — Other specified diseases of pancreas
• lipoprotein (familial) (high density) E78.6 — Lipoprotein deficiency
• liver phosphorylase E74.09 — Other glycogen storage disease
• lysosomal alpha-1, 4 glucosidase E74.02 — Pompe disease
• lysosome-associated membrane protein 2 [LAMP2] E74.05 — Lysosome-associated membrane protein 2 [LAMP2] deficiency
• magnesium E61.2 — Magnesium deficiency
• major histocompatibility complex
• class I D81.6 — Major histocompatibility complex class I deficiency
• class II D81.7 — Major histocompatibility complex class II deficiency
• manganese E61.3 — Manganese deficiency
• MCAD (medium chain acyl CoA dehydrogenase deficiency) E71.311 — Medium chain acyl CoA dehydrogenase deficiency
• menadione (vitamin K) E56.1 — Deficiency of vitamin K
• newborn P53 — Hemorrhagic disease of newborn
• mental (familial) (hereditary)
• methylenetetrahydrofolate reductase (MTHFR) E72.12 — Methylenetetrahydrofolate reductase deficiency
• mevalonate kinase M04.1 — Periodic fever syndromes
• mineral NEC E61.8 — Deficiency of other specified nutrient elements
• mineralocorticoid E27.49 — Other adrenocortical insufficiency
• with glucocorticoid E27.49 — Other adrenocortical insufficiency
• molybdenum (nutritional) E61.5 — Molybdenum deficiency
• moral F60.2 — Antisocial personality disorder
• multiple nutrient elements E61.7 — Deficiency of multiple nutrient elements
• multiple sulfatase (MSD) E75.26 — Sulfatase deficiency
• muscle
• carnitine (palmityltransferase) E71.314 — Muscle carnitine palmitoyltransferase deficiency
• phosphofructokinase E74.09 — Other glycogen storage disease
• myoadenylate deaminase E79.2 — Myoadenylate deaminase deficiency
• myocardial
• myophosphorylase E74.04 — McArdle disease
• NADH diaphorase or reductase (congenital) D74.0 — Congenital methemoglobinemia
• NADH-methemoglobin reductase (congenital) D74.0 — Congenital methemoglobinemia
• natrium E87.1 — Hypo-osmolality and hyponatremia
• niacin (amide) (-tryptophan) E52 — Niacin deficiency [pellagra]
• nicotinamide E52 — Niacin deficiency [pellagra]
• nicotinic acid E52 — Niacin deficiency [pellagra]
• number of teeth
• nutrient element E61.9 — Deficiency of nutrient element, unspecified
• multiple E61.7 — Deficiency of multiple nutrient elements
• specified NEC E61.8 — Deficiency of other specified nutrient elements
• nutrition, nutritional E63.9 — Nutritional deficiency, unspecified
• sequelae
• specified NEC E63.8 — Other specified nutritional deficiencies
• of interleukin 1 receptor antagonist [DIRA] M04.8 — Other autoinflammatory syndromes
• ornithine transcarbamylase E72.4 — Disorders of ornithine metabolism
• ovarian E28.39 — Other primary ovarian failure
• oxygen
• pantothenic acid E53.8 — Deficiency of other specified B group vitamins
• parathyroid (gland) E20.9 — Hypoparathyroidism, unspecified
• perineum (female) N81.89 — Other female genital prolapse
• phenylalanine hydroxylase E70.1 — Other hyperphenylalaninemias
• phosphoenolpyruvate carboxykinase E74.4 — Disorders of pyruvate metabolism and gluconeogenesis
• phosphofructokinase E74.19 — Other disorders of fructose metabolism
• phosphomannomutase E74.818 — Other disorders of glucose transport
• phosphomannose isomerase E74.818 — Other disorders of glucose transport
• phosphomannosyl mutase E74.818 — Other disorders of glucose transport
• phosphorylase kinase, liver E74.09 — Other glycogen storage disease
• pituitary hormone (isolated) E23.0 — Hypopituitarism
• plasma thromboplastin
• antecedent (PTA) D68.1 — Hereditary factor XI deficiency
• component (PTC) D67 — Hereditary factor IX deficiency
• plasminogen (type 1) (type 2) E88.02 — Plasminogen deficiency
• platelet NEC D69.19 — Other qualitative platelet defects
• constitutional
• polyglandular E31.8 — Other polyglandular dysfunction
• autoimmune E31.0 — Autoimmune polyglandular failure
• potassium (K) E87.6 — Hypokalemia

See all 417 entries in the alphabetic index

What is the ICD-10 code for 3-beta hydroxysteroid dehydrogenase deficiency?

E25.0 — Congenital adrenogenital disorders associated with enzyme deficiency.

What is the ICD-10 code for 5-alpha reductase deficiency?

E29.1 — Testicular hypofunction.

What is the ICD-10 code for 11-hydroxylase deficiency?

E25.0 — Congenital adrenogenital disorders associated with enzyme deficiency.

What is the ICD-10 code for 21-hydroxylase deficiency?

E25.0 — Congenital adrenogenital disorders associated with enzyme deficiency.

What is the ICD-10 code for aadc deficiency?

E70.81 — Aromatic L-amino acid decarboxylase deficiency.

What is the ICD-10 code for abdominal muscle syndrome deficiency?

Q79.4 — Prune belly syndrome.

What is the ICD-10 code for accelerator globulin deficiency?

D68.2 — Hereditary deficiency of other clotting factors.