3-beta hydroxysteroid dehydrogenaseE25.0

5-alpha reductase E29.1

11-hydroxylaseE25.0

21-hydroxylaseE25.0

AADC E70.81

abdominal muscle syndromeQ79.4

accelerator globulin D68.2

AC globulin D68.2

acquiredD68.4

acid phosphataseE83.39

acid sphingomyelinase E75.249

type

AE75.240

A/BE75.244

BE75.241

activating factor D68.2

ADA2 D81.32

adenosine deaminase D81.30

with severe combined immunodeficiency D81.31

partial D81.39

specified NECD81.39

type 1 D81.39

type 2D81.32

aldolase E74.19

alpha-1-antitrypsinE88.01

amino-acidsE72.9

anemia, see [Anemia]

aneurinE51.9

antibody with

hyperimmunoglobulinemiaD80.6

near-normal immunoglobinsD80.6

antidiuretic hormoneE23.2

anti-hemophilic

factor D66

BD67

CD68.1

globulin NECD66

antithrombin D68.59

aromatic L-amino acid decarboxylase E70.81

ascorbic acidE54

attention F98.8

with hyperactivity, see [Disorder, attention-deficit hyperactivity]

autoprothrombin

ID68.2

IID67

CD68.2

beta-glucuronidaseE76.29

biotinE53.8

biotin-dependent carboxylaseD81.819

biotinidaseD81.810

brancher enzyme E74.03

calciferolE55.9

with

adult osteomalaciaM83.8

rickets, see [Rickets]

calcium E58

calorie, severeE43

with marasmusE41

and kwashiorkorE42

cardiac, see [Insufficiency, myocardial]

carnitineE71.40

due to

hemodialysisE71.43

inborn errors of metabolismE71.42

Valproic acid therapyE71.43

iatrogenicE71.43

muscle palmityltransferaseE71.314

primaryE71.41

secondaryE71.448

caroteneE50.9

central nervous systemG96.89

ceruloplasmin E83.01

cholineE53.8

Christmas factorD67

chromiumE61.4

chronic neurovisceral acid sphingomyelinaseE75.244

chronic visceral acid sphingomyelinaseE75.241

clotting , see also [Deficiency, coagulation factor]D68.9

clotting factor NEC , see also [Deficiency, factor]D68.2

coagulation NOSD68.9

with

ectopic pregnancyO08.1

molar pregnancyO08.1

acquired D68.4

antepartum hemorrhage, see [Hemorrhage, antepartum, with coagulation defect]

clotting factor NEC, see also [Deficiency, factor]D68.2

due to

hyperprothrombinemiaD68.4

liver diseaseD68.4

vitamin K deficiencyD68.4

newborn, transientP61.6

postpartumO72.3

specified NECD68.8

cognitiveF09

color visionH53.50

achromatopsiaH53.51

acquiredH53.52

deuteranomalyH53.53

protanomalyH53.54

specified type NECH53.59

tritanomalyH53.55

combined glucocorticoid and mineralocorticoidE27.49

contact factorD68.2

copper E61.0

corticoadrenalE27.40

primaryE27.1

craniofacial axisQ75.009

cyanocobalaminE53.8

C1 esterase inhibitor D84.1

debrancher enzyme E74.03

dehydrogenase

long chain/very long chain acyl CoAE71.310

medium chain acyl CoAE71.311

short chain acyl CoAE71.312

dietE63.9

dihydropyrimidine dehydrogenase E88.89

disaccharidaseE73.9

edema, see [Malnutrition, severe]

endocrineE34.9

energy-supply, see [Malnutrition]

enzymes, circulating NECE88.09

ergosterolE55.9

with

adult osteomalaciaM83.8

rickets, see [Rickets]

essential fatty acid E63.0

eye movements

saccadicH55.81

smooth pursuitH55.82

factor, see also [Deficiency, coagulation]

HagemanD68.2

I D68.2

II D68.2

IX D67

multiple D68.8

acquiredD68.4

V D68.2

VII D68.2

VIII D66

with vascular defect, see [Disease, von Willebrand]

X D68.2

XI D68.1

XII D68.2

XIII D68.2

femoral, proximal focal , see [Defect, reduction, lower limb, longitudinal, femur]

fibrin-stabilizing factor D68.2

acquiredD68.4

fibrinaseD68.2

fibrinogen D68.2

acquiredD65

folateE53.8

folic acidE53.8

foreskinN47.3

fructokinaseE74.11

fructose 1,6-diphosphataseE74.19

fructose-1-phosphate aldolaseE74.19

GABA transaminaseE72.81

GABA-T E72.81

galactokinaseE74.29

galactose-1-phosphate uridyl transferaseE74.29

gammaglobulin in bloodD80.1

hereditaryD80.0

glass factorD68.2

glucocorticoidE27.49

mineralocorticoidE27.49

glucose-6-phosphataseE74.01

glucose-6-phosphate dehydrogenase

anemiaD55.0

without anemiaD75.A

glucose transporter protein type 1E74.810

glucuronyl transferaseE80.5

Glut1E74.810

glycogen synthetaseE74.09

gonadotropin E23.0

growth hormone E23.0

Hageman factorD68.2

hemoglobinD64.9

hepatophosphorylaseE74.09

homogentisate 1,2-dioxygenaseE70.29

hormone

anterior pituitary NECE23.0

growthE23.0

growth E23.0

pituitaryE23.0

testicularE29.1

hypoxanthine- E79.1

immunityD84.9

cell-mediatedD84.89

with thrombocytopenia and eczemaD82.0

combinedD81.9

humoralD80.9

IgA D80.2

IgGD80.3

IgMD80.4

immuno, see [Immunodeficiency]

immunoglobulin, selective

A D80.2

G D80.3

M D80.4

infantile neurovisceral acid sphingomyelinaseE75.240

inositol E53.8

intrinsic

factor D51.0

sphincterN36.42

with urethral hypermobilityN36.43

iodineE61.8

congenital syndrome, see [Syndrome, iodine-deficiency, congenital]

ironE61.1

anemiaD50.9

kaliumE87.6

kappa-light chainD80.8

labile factor D68.2

acquiredD68.4

lacrimal fluid , see also [Syndrome, dry eye]

congenitalQ10.6

lactase

congenitalE73.0

secondaryE73.1

Laki-Lorand factorD68.2

LCAD E71.310

lecithin cholesterol acyltransferaseE78.6

lipocaicK86.89

lipoprotein E78.6

liver phosphorylaseE74.09

lysosomal alpha-1, 4 glucosidaseE74.02

lysosome-associated membrane protein 2 [LAMP2]E74.05

magnesiumE61.2

major histocompatibility complex

class ID81.6

class IID81.7

manganeseE61.3

MCAD E71.311

menadione E56.1

newbornP53

mental , see [Disability, intellectual]

methylenetetrahydrofolate reductase E72.12

mevalonate kinaseM04.1

mineral NECE61.8

mineralocorticoidE27.49

with glucocorticoidE27.49

molybdenum E61.5

moralF60.2

multiple nutrient elementsE61.7

multiple sulfatase E75.26

muscle

carnitine E71.314

phosphofructokinaseE74.09

myoadenylate deaminaseE79.2

myocardial, see [Insufficiency, myocardial]

myophosphorylaseE74.04

NADH diaphorase or reductase D74.0

NADH-methemoglobin reductase D74.0

natriumE87.1

niacin E52

nicotinamideE52

nicotinic acidE52

number of teeth, see [Anodontia]

nutrient elementE61.9

multipleE61.7

specified NECE61.8

nutrition, nutritional, see also [Nutrition deficient]E63.9

sequelae, see [Sequelae, nutritional deficiency]

specified NECE63.8

of interleukin 1 receptor antagonist [DIRA]M04.8

ornithine transcarbamylaseE72.4

ovarianE28.39

oxygen, see [Anoxia]

pantothenic acidE53.8

parathyroid E20.9

perineum N81.89

phenylalanine hydroxylaseE70.1

phosphoenolpyruvate carboxykinaseE74.4

phosphofructokinaseE74.19

phosphomannomutuseE74.818

phosphomannose isomeraseE74.818

phosphomannosyl mutaseE74.818

phosphorylase kinase, liverE74.09

pituitary hormone E23.0

plasma thromboplastin

antecedent D68.1

component D67

plasminogen E88.02

platelet NECD69.1

constitutional, see [Disease, von Willebrand]

polyglandularE31.8

autoimmuneE31.0

potassium E87.6

prepuceN47.3

proaccelerin D68.2

acquiredD68.4

proconvertin factor D68.2

acquiredD68.4

protein, see also [Malnutrition]E46

anemiaD53.0

CD68.59

SD68.59

prothrombin D68.2

acquiredD68.4

Prower factorD68.2

pseudocholinesteraseE88.09

PTA D68.1

PTC D67

purine nucleoside phosphorylase D81.5

pyracin E53.1

pyridoxalE53.1

pyridoxamineE53.1

pyridoxine E53.1

pyruvate

carboxylaseE74.4

dehydrogenaseE74.4

riboflavin E53.0

saltE87.1

SCAD E71.312

secretion

ovaryE28.39

salivary gland K11.7

urineR34

selenium E59

serum antitrypsin, familialE88.01

short stature homeobox gene

with

dyschondrosteosisQ78.8

short stature E34.328

Turner's syndromeQ96.9

sodium E87.1

SPCA D68.2

sphincter, intrinsicN36.42

with urethral hypermobilityN36.43

stable factor D68.2

acquiredD68.4

Stuart-Prower D68.2

succinic semialdehyde dehydrogenaseE72.81

sucraseE74.39

sulfataseE75.26

sulfite oxidaseE72.19

thiamin, thiaminic E51.9

beriberi E51.11

wetE51.12

thrombokinaseD68.2

newbornP53

thyroid , see [Hypothyroidism]

tocopherolE56.0

tooth budK00.0

transcobalamine II D51.2

vanadiumE61.6

vascularI99.9

vasopressinE23.2

vertical ridgeK06.8

viosterol, see [Deficiency, calciferol]

vitamin NOSE56.9

AE50.9

with

Bitot's spot (corneal)E50.1

follicular keratosisE50.8

keratomalaciaE50.4

manifestations NECE50.8

night blindnessE50.5

scar of cornea, xerophthalmicE50.6

xerodermaE50.8

xerophthalmiaE50.7

xerosis

conjunctivalE50.0

and Bitot's spotE50.1

corneaE50.2

and ulcerationE50.3

sequelaeE64.1

B NOSE53.9

with

beriberi (dry)E51.11

wetE51.12

pellagraE52

B1 NOSE51.9

beriberi E51.11

with circulatory system manifestationsE51.11

wetE51.12

B12E53.8

B2 E53.0

B6E53.1

CE54

sequelaeE64.2

DE55.9

with

adult osteomalaciaM83.8

rickets, see [Rickets]

25-hydroxylaseE83.32

EE56.0

folic acidE53.8

GE53.0

group BE53.9

specified NECE53.8

H E53.8

KE56.1

of newbornP53

nicotinicE52

PE56.8

PP E52

specified NECE56.8

thiaminE51.9

beriberi, see [Beriberi]

VLCAD E71.310

von Willebrand factor

partial quantitative, see also [Disease, von Willebrand]D68.01

total quantitative, see also [Disease, von Willebrand]D68.03

zinc, dietaryE60