Alphabetic index · D

Deficiency, deficient

Sub-terms

3-beta hydroxysteroid dehydrogenaseE25.0
5-alpha reductase (with male pseudohermaphroditism)E29.1
11-hydroxylaseE25.0
21-hydroxylaseE25.0
AADC (aromatic L-amino acid decarboxylase)E70.81
ABCC6
causing generalized arterial calcification of infancyE83.823
pseudoxanthoma elasticumE83.824
abdominal muscle syndromeQ79.4
accelerator globulin (Ac G) (blood)D68.2
AC globulin (congenital) (hereditary)D68.2
acquiredD68.4
acid phosphataseE83.39
acid sphingomyelinase (ASMD)E75.249
type
AE75.240
A/BE75.244
BE75.241
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 NECD81.39
type 1 (without SCID) (without severe combined immunodeficiency)D81.39
type 2D81.32
aldolase (hereditary)E74.19
alpha-1-antitrypsinE88.01
amino-acidsE72.9
anemiasee Anemia
aneurinE51.9
antibody with
hyperimmunoglobulinemiaD80.6
near-normal immunoglobinsD80.6
antidiuretic hormoneE23.2
anti-hemophilic
factor (A)D66
BD67
CD68.1
globulin (AHG) NECD66
antithrombin (antithrombin III)D68.59
aromatic L-amino acid decarboxylase (AADC)E70.81
ascorbic acidE54
attention (disorder) (syndrome)F98.8
with hyperactivitysee Disorder, attention-deficit hyperactivity
autoprothrombin
ID68.2
IID67
CD68.2
beta-glucuronidaseE76.29
biotinE53.8
biotin-dependent carboxylaseD81.819
biotinidaseD81.810
brancher enzyme (amylopectinosis)E74.03
calciferolE55.9
with
adult osteomalaciaM83.8
ricketssee Rickets
calcium (dietary)E58
calorie, severeE43
with marasmusE41
and kwashiorkorE42
cardiacsee 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
CD73 deficiency causing arterial calcificationE83.825
central nervous systemG96.89
ceruloplasmin (Wilson)E83.01
cholineE53.8
Christmas factorD67
chromiumE61.4
chronic neurovisceral acid sphingomyelinaseE75.244
chronic visceral acid sphingomyelinaseE75.241
clotting (blood)see also Deficiency, coagulation factorD68.9
clotting factor NEC (hereditary)see also Deficiency, factorD68.2
coagulation NOSD68.9
with
ectopic pregnancyO08.1
molar pregnancyO08.1
acquired (any)D68.4
antepartum hemorrhagesee Hemorrhage, antepartum, with coagulation defect
clotting factor NECsee also Deficiency, factorD68.2
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 (nutritional)E61.0
corticoadrenalE27.40
primaryE27.1
craniofacial axisQ75.009
cyanocobalaminE53.8
C1 esterase inhibitor (C1-INH)D84.1
debrancher enzyme (limit dextrinosis)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 (DPD)E88.89
disaccharidaseE73.9
edemasee Malnutrition, severe
endocrineE34.9
energy-supplysee Malnutrition
ENPP1
causing
autosomal recessive hypophosphatemic rickets type 2E83.822
generalized arterial calcification of infancyE83.821
enzymes, circulating NECE88.09
ergosterolE55.9
with
adult osteomalaciaM83.8
ricketssee Rickets
essential fatty acid (EFA)E63.0
eye movements
saccadicH55.81
smooth pursuitH55.82
factorsee also Deficiency, coagulation
HagemanD68.2
I (congenital) (hereditary)D68.2
II (congenital) (hereditary)D68.2
IX (congenital) (functional) (hereditary) (with functional defect)D67
multiple (congenital)D68.8
acquiredD68.4
V (congenital) (hereditary)D68.2
VII (congenital) (hereditary)D68.2
VIII (congenital) (functional) (hereditary) (with functional defect)D66
with vascular defectsee 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
acquiredD68.4
fibrinaseD68.2
fibrinogen (congenital) (hereditary)D68.2
acquiredD65
folateE53.8
folic acidE53.8
foreskinN47.3
fructokinaseE74.11
fructose 1,6-diphosphataseE74.19
fructose-1-phosphate aldolaseE74.19
GABA (gamma aminobutyric acid) transaminaseE72.81
GABA-T (gamma aminobutyric acid transaminase)E72.81
GABA transporter 1QA0.0131
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 (isolated)E23.0
growth hormone (idiopathic) (isolated)E23.0
Hageman factorD68.2
hemoglobinD64.9
hepatophosphorylaseE74.09
homogentisate 1,2-dioxygenaseE70.29
hormone
anterior pituitary (partial) NECE23.0
growthE23.0
growth (isolated)E23.0
pituitaryE23.0
testicularE29.1
hypoxanthine- (guanine)-phosphoribosyltransferase (HG- PRT) (total H-PRT)E79.1
immunityD84.9
cell-mediatedD84.89
with thrombocytopenia and eczemaD82.0
combinedD81.9
humoralD80.9
IgA (secretory)D80.2
IgGD80.3
IgMD80.4
immunosee Immunodeficiency
immunoglobulin, selective
A (IgA)D80.2
G (IgG) (subclasses)D80.3
M (IgM)D80.4
infantile neurovisceral acid sphingomyelinaseE75.240
inositol (B complex)E53.8
intrinsic
factor (congenital)D51.0
sphincterN36.42
with urethral hypermobilityN36.43
iodineE61.8
congenital syndromesee Syndrome, iodine-deficiency, congenital
ironE61.1
anemiaD50.9
kaliumE87.6
kappa-light chainD80.8
labile factor (congenital) (hereditary)D68.2
acquiredD68.4
lacrimal fluid (acquired)see also Syndrome, dry eye
congenitalQ10.6
lactase
congenitalE73.0
secondaryE73.1
Laki-Lorand factorD68.2
LCAD (long chain acyl CoA dehydrogenase deficiency)E71.310
lecithin cholesterol acyltransferaseE78.6
leukocyte adhesion (LAD-I) (LAD-II) (LAD-III)D71.1
type ID71.1
type IID71.1
type IIID71.1
lipocaicK86.89
lipoprotein (familial) (high density)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 (medium chain acyl CoA dehydrogenase deficiency)E71.311
menadione (vitamin K)E56.1
newbornP53
mental (familial) (hereditary)see Disability, intellectual
methylenetetrahydrofolate reductase (MTHFR)E72.12
mevalonate kinaseM04.1
mineral NECE61.8
mineralocorticoidE27.49
with glucocorticoidE27.49
molybdenum (nutritional)E61.5
moralF60.2
multiple nutrient elementsE61.7
multiple sulfatase (MSD)E75.26
muscle
carnitine (palmityltransferase)E71.314
phosphofructokinaseE74.09
myoadenylate deaminaseE79.2
myocardialsee Insufficiency, myocardial
myophosphorylaseE74.04
NADH diaphorase or reductase (congenital)D74.0
NADH-methemoglobin reductase (congenital)D74.0
natriumE87.1
niacin (amide) (-tryptophan)E52
nicotinamideE52
nicotinic acidE52
number of teethsee Anodontia
nutrient elementE61.9
multipleE61.7
specified NECE61.8
nutrition, nutritionalsee also Nutrition deficientE63.9
sequelaesee Sequelae, nutritional deficiency
specified NECE63.8
of interleukin 1 receptor antagonist [DIRA]M04.8
ornithine transcarbamylaseE72.4
ovarianE28.39
oxygensee Anoxia
pantothenic acidE53.8
parathyroid (gland)E20.9
perineum (female)N81.89
phenylalanine hydroxylaseE70.1
phosphoenolpyruvate carboxykinaseE74.4
phosphofructokinaseE74.19
phosphomannomutaseE74.818
phosphomannose isomeraseE74.818
phosphomannosyl mutaseE74.818
phosphorylase kinase, liverE74.09
pituitary hormone (isolated)E23.0
plasma thromboplastin
antecedent (PTA)D68.1
component (PTC)D67
plasminogen (type 1) (type 2)E88.02
platelet NECD69.1
constitutionalsee Disease, von Willebrand
polyglandularE31.8
autoimmuneE31.0
potassium (K)E87.6
prepuceN47.3
proaccelerin (congenital) (hereditary)D68.2
acquiredD68.4
proconvertin factor (congenital) (hereditary)D68.2
acquiredD68.4
proteinsee also MalnutritionE46
anemiaD53.0
CD68.59
SD68.59
prothrombin (congenital) (heredItary)D68.2
acquiredD68.4
Prower factorD68.2
pseudocholinesteraseE88.09
PTA (plasma thromboplastin antecedent)D68.1
PTC (plasma thromboplastin component)D67
purine nucleoside phosphorylase (PNP)D81.5
pyracin (alpha) (beta)E53.1
pyridoxalE53.1
pyridoxamineE53.1
pyridoxine (derivatives)E53.1
pyruvate
carboxylaseE74.4
dehydrogenaseE74.4
riboflavin (vitamin B2)E53.0
saltE87.1
SCAD (short chain acyl CoA dehydrogenase deficiency)E71.312
secretion
ovaryE28.39
salivary gland (any)K11.7
urineR34
selenium (dietary)E59
serum antitrypsin, familialE88.01
short stature homeobox gene (SHOX)
with
dyschondrosteosisQ78.8
short stature (idiopathic)E34.328
Turner's syndromeQ96.9
sodium (Na)E87.1
SPCA (factor VII)D68.2
sphincter, intrinsicN36.42
with urethral hypermobilityN36.43
stable factor (congenital) (hereditary)D68.2
acquiredD68.4
Stuart-Prower (factor X)D68.2
succinic semialdehyde dehydrogenaseE72.81
sucraseE74.39
sulfataseE75.26
sulfite oxidaseE72.19
thiamin, thiaminic (chloride)E51.9
beriberi (dry)E51.11
wetE51.12
thrombokinaseD68.2
newbornP53
thyroid (gland)see Hypothyroidism
tocopherolE56.0
tooth budK00.0
transcobalamine II (anemia)D51.2
vanadiumE61.6
vascularI99.9
vasopressinE23.2
vertical ridgeK06.8
viosterolsee Deficiency, calciferol
vitamin (multiple) 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 (complex) NOSE53.9
with
beriberi (dry)E51.11
wetE51.12
pellagraE52
B1 NOSE51.9
beriberi (dry)E51.11
with circulatory system manifestationsE51.11
wetE51.12
B12E53.8
B2 (riboflavin)E53.0
B6E53.1
CE54
sequelaeE64.2
DE55.9
with
adult osteomalaciaM83.8
ricketssee Rickets
25-hydroxylaseE83.32
EE56.0
folic acidE53.8
GE53.0
group BE53.9
specified NECE53.8
H (biotin)E53.8
KE56.1
of newbornP53
nicotinicE52
PE56.8
PP (pellagra-preventing)E52
specified NECE56.8
thiaminE51.9
beriberisee Beriberi
VLCAD (very long chain acyl CoA dehydrogenase deficiency)E71.310
von Willebrand factor
partial quantitativesee also Disease, von WillebrandD68.01
total quantitativesee also Disease, von WillebrandD68.03
zinc, dietaryE60

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