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Deficiency ICD-10-CM Alphabetical Index

The ICD-10-CM Alphabetical Index is designed to allow medical coders to look up various medical terms and connect them with the appropriate ICD codes. There are 190 terms under the parent term 'Deficiency' in the ICD-10-CM Alphabetical Index.


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
factor (A) D66
B D67
C D68.1
globulin (AHG) NEC D66
antithrombin (antithrombin III) D68.59
ascorbic acid E54
attention (disorder) (syndrome) F98.8
with hyperactivity - see Disorder, attention-deficit hyperactivity
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
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) D68.9 - see also Deficiency, coagulation factor
clotting factor NEC (hereditary) D68.2 - see also Deficiency, factor
coagulation NOS D68.9
ectopic pregnancy O08.1
molar pregnancy O08.1
acquired (any) D68.4
antepartum hemorrhage - see Hemorrhage, antepartum, with coagulation defect
clotting factor NEC D68.2 - see also Deficiency, factor
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
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
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
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
anterior pituitary (partial) NEC 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
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
congenital E73.0
secondary E73.1
Laki-Lorand factor D68.2
lecithin cholesterol acyltransferase E78.6
lipocaic K86.8
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
mineral NEC E61.8
mineralocorticoid E27.49
with glucocorticoid E27.49
molybdenum (nutritional) E61.5
moral F60.2
multiple nutrient elements E61.7
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
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
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 E46 - see also Malnutrition
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
carboxylase E74.4
dehydrogenase E74.4
riboflavin (vitamin B2) E53.0
salt E87.1
ovary E28.39
salivary gland (any) K11.7
urine R34
selenium (dietary) E59
serum antitrypsin, familial E88.01
short stature homeobox gene (SHOX)
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
sucrase E74.39
sulfatase E75.29
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
viosterol - see Deficiency, calciferol
vitamin (multiple) NOS E56.9
A E50.9
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
conjunctival E50.0
and Bitot's spot E50.1
cornea E50.2
and ulceration E50.3
sequelae E64.1
B (complex) NOS E53.9
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
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
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Source: http://icd.codes/icd10cm/alphabetical-index/deficiency