Alphabetic Index · main term

Deficiency, deficient

FY2027Index: De /Alphabetic Index

Deficiency, deficient is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). It has 417 subterms and 362 code entries. First-level subterms include 3-beta hydroxysteroid dehydrogenase, 5-alpha reductase, 11-hydroxylase, 21-hydroxylase, AADC, ABCC6, abdominal muscle syndrome, accelerator globulin and more. Confirm any code you find here in the Tabular List before you report it.

Subterms 417

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
anemia see 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 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 (amylopectinosis)E74.03
calciferolE55.9
- with
  - adult osteomalaciaM83.8
  - rickets see Rickets
calcium (dietary)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
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 hemorrhage see Hemorrhage, antepartum, with coagulation defect
- clotting factor NEC see 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
edema see Malnutrition, severe
endocrineE34.9
energy-supply see 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
  - rickets see Rickets
essential fatty acid (EFA)E63.0
eye movements
- saccadicH55.81
- smooth pursuitH55.82
factor see 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 defect see 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
immuno see 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 syndrome see 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
myocardial see 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 teeth see Anodontia
nutrient elementE61.9
- multipleE61.7
- specified NECE61.8
nutrition, nutritional see also Nutrition deficientE63.9
- 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 (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 NECD69.19
- constitutional see 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
protein see 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
viosterol see 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
    rickets see 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
  - beriberi see Beriberi
VLCAD (very long chain acyl CoA dehydrogenase deficiency)E71.310
von Willebrand factor
- partial quantitative see also Disease, von WillebrandD68.01
- total quantitative see also Disease, von WillebrandD68.03
zinc, dietaryE60