Browse Disease Index: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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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) 286.3 See also: Defect, coagulation
AC globulin (congenital) 286.3 See also: Defect, coagulation
acquired 286.7
activating factor (blood) 286.3 See also: Defect, coagulation
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
with beriberi 265
antibody NEC 279.00
antidiuretic hormone 253.5
antihemophilic
factor (A) 286
B 286.1
C 286.2
globulin (AHG) NEC 286
antithrombin III 289.81
antitrypsin 273.4
argininosuccinate synthetase or lyase 270.6
ascorbic acid (with scurvy) 267
autoprothrombin
I 286.3 See also: Defect, coagulation
II 286.1
C 286.3 See also: Defect, coagulation
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 268 See also: Rickets
calcium 275.40
dietary 269.3
calorie, severe 261
carbamyl phosphate synthetase 270.6
cardiac 428.0 See also: Insufficiency, myocardial
carnitine 277.81
due to
hemodialysis 277.83
inborn errors of metabolism 277.82
valproic acid therapy 277.83
iatrogenic 277.83
palmitoyltransferase (CPT1, CPT2) 277.85
palmityl transferase (CPT1, CPT2) 277.85
primary 277.81
secondary 277.84
carotene 264.9
Carr factor 286.9 See also: Defect, coagulation
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) 286.9 See also: Defect, coagulation
coagulation factor NEC 286.9
with
abortion See: Abortion, by type, with hemorrhage
ectopic pregnancy 639.1 See also: categories 634-638
molar pregnancy 639.1 See also: categories 630-632
acquired (any) 286.7
antepartum or intrapartum 641.3
affecting fetus or newborn 762.1
complicating pregnancy, childbirth, or puerperium 649.3
due to
liver disease 286.7
vitamin K deficiency 286.7
newborn, transient 776.3
postpartum 666.3
specified type NEC 286.3
color vision (congenital) 368.59
acquired 368.55
combined, two or more coagulation factors 286.9 See also: Defect, coagulation
complement factor NEC 279.8
contact factor 286.3 See also: Defect, coagulation
copper NEC 275.1
corticoadrenal 255.4
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
dihydropteridine reductase 270.1
disaccharidase (intestinal) 271.3
disease NEC 269.9
ear(s) V48.8
edema 262
endocrine 259.9
enzymes, circulating NEC 277.6 See also: Deficiency, by specific enzyme
ergosterol 268.9
with
osteomalacia 268.2
rickets 268 See also: Rickets
erythrocytic glutathione (anemia) 282.2
eyelid(s) V48.8
factor 286.9 See also: Defect, coagulation
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
with
functional defect 286
vascular defect 286.4
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
acquired 286.7
fibrinase 286.3 See also: Defect, coagulation
fibrinogen (congenital) 286.3 See also: Defect, coagulation
acquired 286.6
fibrin-stabilizing factor (congenital) 286.3 See also: Defect, coagulation
acquired 286.7
finger See: Absence, finger
fletcher factor 286.9 See also: Defect, coagulation
fluorine 269.3
folate, anemia 281.2
folic acid (vitamin BC) 266.2
anemia 281.2
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 286.3 See also: Defect, coagulation
glucocorticoid 255.4
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) 286.3 See also: Defect, coagulation
head V48.0
hemoglobin 285.9 See also: Anemia
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
growth (human) 253.3
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
hyper-IgM 279.05
autosomal recessive 279.05
X-linked 279.05
increased IgM 279.05
congenital hypogammaglobulinemia 279.04
non-sex-linked 279.06
selective immunoglobulin NEC 279.03
IgA 279.01
IgG 279.03
IgM 279.02
increased 279.05
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
cell-mediated 279.1
with
hyperimmunoglobulinemia 279.2
thrombocytopenia and eczema 279.12
specified NEC 279.19
combined (severe) 279.2
syndrome 279.2
common variable 279.06
humoral NEC 279
IgA (secretory) 279.01
IgG 279.03
IgM 279.02
immunoglobulin, selective NEC 279.03
IgA 279.01
IgG 279.03
IgM 279.02
inositol (B complex) 266.2
interferon 279.4
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) 286.3 See also: Defect, coagulation
acquired 286.7
lacrimal fluid (acquired) 375.15
congenital 743.64
lactase 271.3
laki-Lorand factor 286.3 See also: Defect, coagulation
lecithin-cholesterol acyltranferase 272.5
LH (luteinizing hormone) 253.4
limb V49.0
lower V49.0
congenital 755.3 See also: Deficiency, lower limb, congenital
upper V49.0
congenital 755.2 See also: Deficiency, upper limb, congenital
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 755.3
with complete absence of distal elements 755.31
longitudinal (complete) (partial) (with distal deficiencies, incomplete) 755.32
with complete absence of distal elements 755.31
combined femoral, tibial, fibular (incomplete) 755.33
femoral 755.34
fibular 755.37
metatarsal(s) 755.38
phalange(s) 755.39
meaning all digits 755.31
tarsal(s) 755.38
tibia 755.36
tibiofibular 755.35
transverse 755.31
luteinizing hormone (LH) 253.4
lysosomal alpha-1, 4 glucosidase 271
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
newborn 776
mental (familial) (hereditary) 319 See also: Retardation, mental
mineral NEC 269.3
molybdenum 269.3
moral 301.7
multiple, syndrome 260
myocardial 428.0 See also: Insufficiency, myocardial
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 520.0 See also: Anodontia
nutrition, nutritional 269.9
specified NEC 269.8
ornithine transcarbamylase 270.6
ovarian 256.39
oxygen 799.02 See also: Anoxia
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
posterior 253.5
placenta See: Placenta, insufficiency
plasma
cell 279
protein (paraproteinemia) (pyroglobulinemia) 273.8
gamma globulin 279
thromboplastin
antecedent (PTA) 286.2
component (PTC) 286.1
platelet NEC 287.1
constitutional 286.4
polyglandular 258.9
potassium (K) 276.8
proaccelerin (congenital) 286.3 See also: Defect, congenital
acquired 286.7
proconvertin factor (congenital) 286.3 See also: Defect, coagulation
acquired 286.7
prolactin 253.4
protein 260
anemia 281.4
C 289.81
plasma See: Deficiency, plasma, protein
S 289.81
prothrombin (congenital) 286.3 See also: Defect, coagulation
acquired 286.7
Prower factor 286.3 See also: Defect, coagulation
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
ovary 256.39
salivary gland (any) 527.7
urine 788.5
selenium 269.3
serum
antitrypsin, familial 273.4
protein (congenital) 273.8
short chain acyl CoA dehydrogenase (SCAD) 277.85
smooth pursuit movements (eye) 379.58
sodium (Na) 276.1
SPCA 286.3 See also: Defect, coagulation
specified NEC 269.8
stable factor (congenital) 286.3 See also: Defect, coagulation
acquired 286.7
Stuart (-Prower) factor 286.3 See also: Defect, coagulation
sucrase 271.3
sucrase-isomaltase 271.3
sulfite oxidase 270.0
syndrome, multiple 260
thiamine, thiaminic (chloride) 265.1
thrombokinase 286.3 See also: Defect, coagulation
newborn 776
thrombopoieten 287.39
thymolymphatic 279.2
thyroid (gland) 244.9
tocopherol 269.1
toe See: Absence, toe
tooth bud 520.0 See also: Anodontia
trunk V48.1
UDPG-glycogen transferase 271.0
upper limb V49.0
congenital 755.2
with complete absence of distal elements 755.21
longitudinal (complete) (partial) (with distal deficiencies, incomplete) 755.22
carpal(s) 755.28
combined humeral, radial, ulnar (incomplete) 755.23
humeral 755.24
metacarpal(s) 755.28
phalange(s) 755.29
meaning all digits 755.21
radial 755.26
radioulnar 755.25
ulnar 755.27
transverse (complete) (partial) 755.21
vascular 459.9
vasopressin 253.5
viosterol 268.9 See also: Deficiency, calciferol
vitamin (multiple) NEC 269.2
A 264.9
with
Bitôt's spot 264.1
corneal 264.2
with corneal ulceration 264.3
keratomalacia 264.4
keratosis, follicular 264.8
night blindness 264.5
scar of cornea, xerophthalmic 264.6
specified manifestation NEC 264.8
ocular 264.7
xeroderma 264.8
xerophthalmia 264.7
xerosis
conjunctival 264
with Bitôt's spot 264.1
corneal 264.2
with corneal ulceration 264.3
B (complex) NEC 266.9
with
beriberi 265
pellagra 265.2
specified type NEC 266.2
B1 NEC 265.1
beriberi 265
B2 266
B6 266.1
B12 266.2
BC (folic acid) 266.2
C (ascorbic acid) (with scurvy) 267
D (calciferol) (ergosterol) 268.9
with
osteomalacia 268.2
rickets 268 See also: Rickets
E 269.1
folic acid 266.2
G 266
H 266.2
K 269
of newborn 776
nicotinic acid 265.2
P 269.1
PP 265.2
specified NEC 269.1
zinc 269.3