Deficiency, deficient
3-beta hydroxysteroid dehydrogenase
E25.0 5-alpha reductase (with male pseudohermaphroditism)
E29.1 11-hydroxylase
E25.0 21-hydroxylase
E25.0 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 activating factor (blood)
D68.2 adenosine deaminase (ADA)
D81.3 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 NEC (AHG)
D66 antithrombin (antithrombin III)
D68.59 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 central nervous system
G96.8 ceruloplasmin (Wilson)
E83.01 choline
E53.8 Christmas factor
D67 chromium
E61.4 clotting (blood) --see also Deficiency, coagulation factor
D68.9 clotting factor NEC (hereditary) --see also Deficiency, factor
D68.2 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 --see also Deficiency, factor
D68.2 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
Q75.0 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 enzymes, circulating NEC
E88.09 ergosterol
E55.9 with
adult osteomalacia
M83.8 rickets
--see Rickets essential fatty acid (EFA)
E63.0 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
D68.0 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 transaminase (gamma aminobutyric acid)
E72.81 GABA-T (gamma aminobutyric acid transaminase)
E72.81 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 glucuronyl transferase
E80.5 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 NEC (partial)
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
D84.8 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 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 lecithin cholesterol acyltransferase
E78.6 lipocaic
K86.89 lipoprotein (familial) (high density)
E78.6 liver phosphorylase
E74.09 lysosomal alpha-1, 4 glucosidase
E74.02 magnesium
E61.2 major histocompatibility complex
class I
D81.6 class II
D81.7 manganese
E61.3 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 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 phosphomannomutuse
E74.8 phosphomannose isomerase
E74.8 phosphomannosyl mutase
E74.8 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
D69.1 constitutional
D68.0 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 --see also Malnutrition
E46 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 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)
E34.3 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 NOS (multiple)
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 NOS (complex)
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 zinc, dietary
E60