Deficiency, deficient
- 3-beta-hydroxysteroid dehydrogenase 255.2
- 6-phosphogluconic dehydrogenase (anemia) 282.2
- 11-beta-hydroxylase 255.2
- 17-alpha-hydroxylase 255.2
- 18-hydroxysteroid dehydrogenase 255.2
- 20-alpha-hydroxylase 255.2
- 21-hydroxylase 255.2
- AAT (alpha-1 antitrypsin) 273.4
- abdominal muscle syndrome 756.79
- accelerator globulin (Ac G) (blood) (see also Defect, coagulation) 286.3
- AC globulin (congenital) (see also Defect, coagulation) 286.3
- activating factor (blood) (see also Defect, coagulation) 286.3
- adenohypophyseal 253.2
- adenosine deaminase 277.2
- aldolase (hereditary) 271.2
- alpha-1-antitrypsin 273.4
- alpha-1-trypsin inhibitor 273.4
- alpha-fucosidase 271.8
- alpha-lipoprotein 272.5
- alpha-mannosidase 271.8
- amino acid 270.9
- anemia - see Anemia, deficiency
- aneurin 265.1
- antibody NEC 279.00
- antidiuretic hormone 253.5
- antihemophilic
- antithrombin III 289.81
- antitrypsin 273.4
- argininosuccinate synthetase or lyase 270.6
- ascorbic acid (with scurvy) 267
- autoprothrombin
- I (see also Defect, coagulation) 286.3
- II 286.1
- C (see also Defect, coagulation) 286.3
- bile salt 579.8
- biotin 266.2
- biotinidase 277.6
- bradykinase-1 277.6
- brancher enzyme (amylopectinosis) 271.0
- calciferol 268.9
- with
- osteomalacia 268.2
- rickets (see also Rickets) 268.0
- calcium 275.40
- calorie, severe 261
- carbamyl phosphate synthetase 270.6
- cardiac (see also Insufficiency, myocardial) 428.0
- carnitine 277.81
- carotene 264.9
- Carr factor (see also Defect, coagulation) 286.9
- central nervous system 349.9
- ceruloplasmin 275.1
- cevitamic acid (with scurvy) 267
- choline 266.2
- Christmas factor 286.1
- chromium 269.3
- citrin 269.1
- clotting (blood) (see also Defect, coagulation) 286.9
- coagulation factor NEC 286.9
- with
- abortion - see Abortion, by type, with hemorrhage
- ectopic pregnancy (see also categories 634-638) 639.1
- molar pregnancy (see also categories 630-632) 639.1
- acquired (any) 286.7
- antepartum or intrapartum 641.3
- affecting fetus or newborn 762.1
- complicating pregnancy, childbirth, or puerperium 649.3
- due to
- newborn, transient 776.3
- postpartum 666.3
- specified type NEC 286.3
- color vision (congenital) 368.59
- combined glucocorticoid and mineralocorticoid 255.41
- combined, two or more coagulation factors (see also Defect, coagulation) 286.9
- complement factor NEC 279.8
- contact factor (see also Defect, coagulation) 286.3
- copper NEC 275.1
- corticoadrenal 255.41
- craniofacial axis 756.0
- cyanocobalamin (vitamin B12) 266.2
- debrancher enzyme (limit dextrinosis) 271.0
- desmolase 255.2
- diet 269.9
- dihydrofolate reductase 281.2
- dihydropyrimidine dehydrogenase (DPD) 277.6
- dihydropteridine reductase 270.1
- disaccharidase (intestinal) 271.3
- disease NEC 269.9
- ear(s) V48.8
- edema 262
- endocrine 259.9
- enzymes, circulating NEC (see also Deficiency, by specific enzyme) 277.6
- ergosterol 268.9
- with
- osteomalacia 268.2
- rickets (see also Rickets) 268.0
- erythrocytic glutathione (anemia) 282.2
- eyelid(s) V48.8
- factor (see also Defect, coagulation) 286.9
- I (congenital) (fibrinogen) 286.3
- antepartum or intrapartum 641.3
- affecting fetus or newborn 762.1
- newborn, transient 776.3
- postpartum 666.3
- II (congenital) (prothrombin) 286.3
- V (congenital) (labile) 286.3
- VII (congenital) (stable) 286.3
- VIII (congenital) (functional) 286.0
- IX (Christmas) (congenital) (functional) 286.1
- X (congenital) (Stuart-Prower) 286.3
- XI (congenital) (plasma thromboplastin antecedent) 286.2
- XII (congenital) (Hageman) 286.3
- XIII (congenital) (fibrin stabilizing) 286.3
- hageman 286.3
- multiple (congenital) 286.9
- fibrinase (see also Defect, coagulation) 286.3
- fibrinogen (congenital) (see also Defect, coagulation) 286.3
- fibrin-stabilizing factor (congenital) (see also Defect, coagulation) 286.3
- finger - see Absence, finger
- fletcher factor (see also Defect, coagulation) 286.9
- fluorine 269.3
- folate, anemia 281.2
- folic acid (vitamin BC) 266.2
- follicle-stimulating hormone (FSH) 253.4
- fructokinase 271.2
- fructose-1, 6-diphosphate 271.2
- fructose-1-phosphate aldolase 271.2
- FSH (follicle-stimulating hormone) 253.4
- fucosidase 271.8
- galactokinase 271.1
- galactose-1-phosphate uridyl transferase 271.1
- gamma globulin in blood 279.00
- glass factor (see also Defect, coagulation) 286.3
- glucocorticoid 255.41
- glucose-6-phosphatase 271.0
- glucose-6-phosphate dehydrogenase anemia 282.2
- glucuronyl transferase 277.4
- glutathione-reductase (anemia) 282.2
- glycogen synthetase 271.0
- growth hormone 253.3
- Hageman factor (congenital) (see also Defect, coagulation) 286.3
- head V48.0
- hemoglobin (see also Anemia) 285.9
- hepatophosphorylase 271.0
- hexose monophosphate (HMP) shunt 282.2
- HGH (human growth hormone) 253.3
- HG-PRT 277.2
- homogentisic acid oxidase 270.2
- hormone - see also Deficiency, by specific hormone
- anterior pituitary (isolated) (partial) NEC 253.4
- follicle-stimulating 253.4
- growth (human) (isolated) 253.3
- human growth 253.3
- interstitial cell-stimulating 253.4
- luteinizing 253.4
- melanocyte-stimulating 253.4
- testicular 257.2
- human growth hormone 253.3
- humoral 279.00
- with
- congenital hypogammaglobulinemia 279.04
- selective immunoglobulin NEC 279.03
- specified NEC 279.09
- hydroxylase 255.2
- hypoxanthine-guanine phosphoribosyltransferase (HG-PRT) 277.2
- ICSH (interstitial cell-stimulating hormone) 253.4
- immunity NEC 279.3
- immunoglobulin, selective NEC 279.03
- inositol (B complex) 266.2
- interferon 279.49
- internal organ V47.0
- interstitial cell-stimulating hormone (ICSH) 253.4
- intrinsic factor (Castle's) (congenital) 281.0
- intrinsic (urethral) sphincter (ISD) 599.82
- invertase 271.3
- iodine 269.3
- iron, anemia 280.9
- labile factor (congenital) (see also Defect, coagulation) 286.3
- lacrimal fluid (acquired) 375.15
- lactase 271.3
- laki-Lorand factor (see also Defect, coagulation) 286.3
- lecithin-cholesterol acyltranferase 272.5
- LH (luteinizing hormone) 253.4
- limb V49.0
- lower V49.0
- congenital (see also Deficiency, lower limb, congenital) 755.30
- upper V49.0
- congenital (see also Deficiency, upper limb, congenital) 755.20
- lipocaic 577.8
- lipoid (high-density) 272.5
- lipoprotein (familial) (high-density) 272.5
- liver phosphorylase 271.0
- long chain 3-hydroxyacyl CoA dehydrogenase (LCHAD) 277.85
- long chain/very long chain acyl CoA dehydrogenase (LCAD, VLCAD) 277.85
- lower limb V49.0
- congenital 755.30
- with complete absence of distal elements 755.31
- longitudinal (complete) (partial) (with distal deficiencies, incomplete) 755.32
- transverse 755.31
- luteinizing hormone (LH) 253.4
- lysosomal alpha-1, 4 glucosidase 271.0
- magnesium 275.2
- mannosidase 271.8
- medium chain acyl CoA dehydrogenase (MCAD) 277.85
- melanocyte-stimulating hormone (MSH) 253.4
- menadione (vitamin K) 269.0
- mental (familial) (hereditary) (see also Disability, intellectual) 319
- methylenetetrahydrofolate reductase (MTHFR) 270.4
- mineral NEC 269.3
- mineralocorticoid 255.42
- molybdenum 269.3
- moral 301.7
- multiple, syndrome 260
- myocardial (see also Insufficiency, myocardial) 428.0
- myophosphorylase 271.0
- NADH (DPNH) -methemoglobin-reductase (congenital) 289.7
- NADH diaphorase or reductase (congenital) 289.7
- neck V48.1
- niacin (amide) (-tryptophan) 265.2
- nicotinamide 265.2
- nicotinic acid (amide) 265.2
- nose V48.8
- number of teeth (see also Anodontia) 520.0
- nutrition, nutritional 269.9
- ornithine transcarbamylase 270.6
- ovarian 256.39
- oxygen (see also Anoxia) 799.02
- pantothenic acid 266.2
- parathyroid (gland) 252.1
- phenylalanine hydroxylase 270.1
- phosphoenolpyruvate carboxykinase 271.8
- phosphofructokinase 271.2
- phosphoglucomutase 271.0
- phosphohexosisomerase 271.0
- phosphomannomutase 271.8
- phosphomannose isomerase 271.8
- phosphomannosyl mutase 271.8
- phosphorylase kinase, liver 271.0
- pituitary (anterior) 253.2
- placenta - see Placenta, insufficiency
- plasma
- cell 279.00
- protein (paraproteinemia) (pyroglobulinemia) 273.8
- thromboplastin
- platelet NEC 287.1
- polyglandular 258.9
- potassium (K) 276.8
- proaccelerin (congenital) (see also Defect, congenital) 286.3
- proconvertin factor (congenital) (see also Defect, coagulation) 286.3
- prolactin 253.4
- protein 260
- prothrombin (congenital) (see also Defect, coagulation) 286.3
- Prower factor (see also Defect, coagulation) 286.3
- PRT 277.2
- pseudocholinesterase 289.89
- psychobiological 301.6
- PTA 286.2
- PTC 286.1
- purine nucleoside phosphorylase 277.2
- pyracin (alpha) (beta) 266.1
- pyridoxal 266.1
- pyridoxamine 266.1
- pyridoxine (derivatives) 266.1
- pyruvate carboxylase 271.8
- pyruvate dehydrogenase 271.8
- pyruvate kinase (PK) 282.3
- riboflavin (vitamin B2) 266.0
- saccadic eye movements 379.57
- salivation 527.7
- salt 276.1
- secretion
- selenium 269.3
- serum
- antitrypsin, familial 273.4
- protein (congenital) 273.8
- short chain acyl CoA dehydrogenase (SCAD) 277.85
- short stature homeobox gene (SHOX)
- smooth pursuit movements (eye) 379.58
- sodium (Na) 276.1
- SPCA (see also Defect, coagulation) 286.3
- specified NEC 269.8
- stable factor (congenital) (see also Defect, coagulation) 286.3
- Stuart (-Prower) factor (see also Defect, coagulation) 286.3
- sucrase 271.3
- sucrase-isomaltase 271.3
- sulfite oxidase 270.0
- syndrome, multiple 260
- thiamine, thiaminic (chloride) 265.1
- thrombokinase (see also Defect, coagulation) 286.3
- thrombopoieten 287.39
- thymolymphatic 279.2
- thyroid (gland) 244.9
- tocopherol 269.1
- toe - see Absence, toe
- tooth bud (see also Anodontia) 520.0
- trunk V48.1
- UDPG-glycogen transferase 271.0
- upper limb V49.0
- congenital 755.20
- with complete absence of distal elements 755.21
- longitudinal (complete) (partial) (with distal deficiencies, incomplete) 755.22
- transverse (complete) (partial) 755.21
- vascular 459.9
- vasopressin 253.5
- viosterol (see also Deficiency, calciferol) 268.9
- vitamin (multiple) NEC 269.2
