Instruction manual part 2e, vol 3: ICD-10 index

INTERNATIONAL CLASSIFICATION OF DISEASES
Deficiency—continued
- fibrin-stabilizing factor (congenital)
(hereditary) D68.2
- - acquired D68.4
- fibrinogen (congenital) (hereditary) D68.2
- - acquired D65
- folate E53.8
- folic acid E53.8
- fructokinase E74.1
- fructose 1,6-diphosphatase E74.1
- galactokinase E74.2
- galactose-1-phosphate uridyl transferase
E74.2
- gammaglobulin in blood D80.1
- - hereditary D80.0
- glucose-6-phosphatase E74.0
- glucose-6-phosphate dehydrogenase anemia
D55.0
- β-glucoronidase E76.2
- glucuronyl transferase E80.5
- glycogen synthetase E74.0
- gonadotropin (isolated) E23.0
- growth hormone (idiopathic) (isolated)
E23.0
- Hageman factor D68.2
- hemoglobin D64.9
- hepatophosphorylase E74.0
- homogentisate 1,2-dioxygenase E70.2
- hormone
- - anterior pituitary (partial) NEC E23.0
- - - growth E23.0
- - growth (isolated) E23.0
- - pituitary E23.0
- - testicular E29.1
- 11-hydroxylase E25.0
- 21-hydroxylase E25.0
- 3β hydroxysteroid dehydrogenase E25.0
- hypoxanthine(-guanine)-
phosphoribosyltransferase (HG-PRT)
(total H-PRT) E79.1
Deficiency—continued
- immunity D84.9
- - cell-mediated D84.8
- - combined D81.9
- - humoral D80.9
- - T-cell D84.8
- immuno - see Immunodeficiency
- immunoglobulin D80.9
- - selective
- - - A (IgA) D80.2
- - - G (IgG) (subclasses) D80.3
- - - M (IgM) D80.4
- immunological D84.9
- intrinsic factor (congenital) D51.0
- invertase E73.1
- iodine E61.8
- - congenital syndrome (see also Syndrome,
iodine-deficiency, congenital) E00.9
- iron E61.1
- iron anemia D50.9
- - secondary to blood loss D50.0
- - - acute D62
- kalium E87.6
- kappa light chain D80.8
- labile factor (congenital) (hereditary) D68.2
- - acquired D68.4
- lacrimal fluid (acquired) H04.1
- - congenital Q10.6
- lactase E73.0
- - congenital E73.0
- - secondary E73.1
- lecithin cholesterol acyltransferase E78.6
- lipocaic K86.8
- lipoprotein (familial) (high density) E78.6
- liver phosphorylase E74.0
- magnesium E61.2
D-8