QA0.0131
BookmarkSLC6A1-related disorder
Filed alongside this entry 186
under Deficiency, deficient
- 3-beta hydroxysteroid dehydrogenase E25.0
- 5-alpha reductase (with male pseudohermaphroditism) E29.1
- 11-hydroxylase E25.0
- 21-hydroxylase E25.0
- AADC (aromatic L-amino acid decarboxylase) E70.81
- abdominal muscle syndrome Q79.4
- accelerator globulin (Ac G) (blood) D68.2
- AC globulin (congenital) (hereditary) D68.2
- acid phosphatase E83.39
- acid sphingomyelinase (ASMD) E75.249
- activating factor (blood) D68.2
- ADA2 (adenosine deaminase 2) D81.32
- adenosine deaminase (ADA) D81.30
- aldolase (hereditary) E74.19
- alpha-1-antitrypsin E88.01
- amino-acids E72.9
- aneurin E51.9
- antidiuretic hormone E23.2
- antithrombin (antithrombin III) D68.59
- aromatic L-amino acid decarboxylase (AADC) E70.81
- ascorbic acid E54
- attention (disorder) (syndrome) F98.8
- beta-glucuronidase E76.29
- biotin E53.8
- biotin-dependent carboxylase D81.819
- biotinidase D81.810
- brancher enzyme (amylopectinosis) E74.03
- calciferol E55.9
- calcium (dietary) E58
- calorie, severe E43
- carnitine E71.40
- carotene E50.9
- CD73 deficiency causing arterial calcification E83.825
- central nervous system G96.89
- ceruloplasmin (Wilson) E83.01
- choline E53.8
- Christmas factor D67
- chromium E61.4
- chronic neurovisceral acid sphingomyelinase E75.244
- chronic visceral acid sphingomyelinase E75.241
- clotting (blood) D68.9
- clotting factor NEC (hereditary) D68.2
- coagulation NOS D68.9
- cognitive F09
- color vision H53.50
- combined glucocorticoid and mineralocorticoid E27.49
- contact factor D68.2
- copper (nutritional) E61.0
- corticoadrenal E27.40
- craniofacial axis Q75.009
- cyanocobalamin E53.8
- C1 esterase inhibitor (C1-INH) D84.1
- debrancher enzyme (limit dextrinosis) E74.03
- diet E63.9
- dihydropyrimidine dehydrogenase (DPD) E88.89
- disaccharidase E73.9
- endocrine E34.9
- enzymes, circulating NEC E88.09
- ergosterol E55.9
- essential fatty acid (EFA) E63.0
- fibrin-stabilizing factor (congenital) (hereditary) D68.2
- fibrinase D68.2
- fibrinogen (congenital) (hereditary) D68.2
- 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
- GABA (gamma aminobutyric acid) transaminase E72.81
- GABA-T (gamma aminobutyric acid transaminase) E72.81
- GABA transporter 1 QA0.0131
- galactokinase E74.29
- galactose-1-phosphate uridyl transferase E74.29
- gammaglobulin in blood D80.1
- glass factor D68.2
- glucocorticoid E27.49
- glucose-6-phosphatase E74.01
- glucose transporter protein type 1 E74.810
- glucuronyl transferase E80.5
- Glut1 E74.810
- 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
- hypoxanthine- (guanine)-phosphoribosyltransferase (HG- PRT) (total H-PRT) E79.1
- immunity D84.9
- infantile neurovisceral acid sphingomyelinase E75.240
- inositol (B complex) E53.8
- iodine E61.8
- iron E61.1
- kalium E87.6
- kappa-light chain D80.8
- labile factor (congenital) (hereditary) D68.2
- Laki-Lorand factor D68.2
- LCAD (long chain acyl CoA dehydrogenase deficiency) E71.310
- lecithin cholesterol acyltransferase E78.6
- leukocyte adhesion (LAD-I) (LAD-II) (LAD-III) D71.1
- lipocaic K86.89
- lipoprotein (familial) (high density) E78.6
- liver phosphorylase E74.09
- lysosomal alpha-1, 4 glucosidase E74.02
- lysosome-associated membrane protein 2 [LAMP2] E74.05
- magnesium E61.2
- manganese E61.3
- MCAD (medium chain acyl CoA dehydrogenase deficiency) E71.311
- menadione (vitamin K) E56.1
- methylenetetrahydrofolate reductase (MTHFR) E72.12
- mevalonate kinase M04.1
- mineral NEC E61.8
- mineralocorticoid E27.49
- molybdenum (nutritional) E61.5
- moral F60.2
- multiple nutrient elements E61.7
- multiple sulfatase (MSD) E75.26
- myoadenylate deaminase E79.2
- 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
- nutrient element E61.9
- nutrition, nutritional E63.9
- of interleukin 1 receptor antagonist [DIRA] M04.8
- ornithine transcarbamylase E72.4
- ovarian E28.39
- pantothenic acid E53.8
- parathyroid (gland) E20.9
- perineum (female) N81.89
- phenylalanine hydroxylase E70.1
- phosphoenolpyruvate carboxykinase E74.4
- phosphofructokinase E74.19
- phosphomannomutase E74.818
- phosphomannose isomerase E74.818
- phosphomannosyl mutase E74.818
- phosphorylase kinase, liver E74.09
- pituitary hormone (isolated) E23.0
- plasminogen (type 1) (type 2) E88.02
- platelet NEC D69.19
- polyglandular E31.8
- potassium (K) E87.6
- prepuce N47.3
- proaccelerin (congenital) (hereditary) D68.2
- proconvertin factor (congenital) (hereditary) D68.2
- protein E46
- prothrombin (congenital) (heredItary) D68.2
- 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
- riboflavin (vitamin B2) E53.0
- salt E87.1
- SCAD (short chain acyl CoA dehydrogenase deficiency) E71.312
- selenium (dietary) E59
- serum antitrypsin, familial E88.01
- sodium (Na) E87.1
- SPCA (factor VII) D68.2
- sphincter, intrinsic N36.42
- stable factor (congenital) (hereditary) D68.2
- Stuart-Prower (factor X) D68.2
- succinic semialdehyde dehydrogenase E72.81
- sucrase E74.39
- sulfatase E75.26
- sulfite oxidase E72.19
- thiamin, thiaminic (chloride) E51.9
- thrombokinase D68.2
- tocopherol E56.0
- tooth bud K00.0
- transcobalamine II (anemia) D51.2
- vanadium E61.6
- vascular I99.9
- vasopressin E23.2
- vertical ridge K06.8
- vitamin (multiple) NOS E56.9
- VLCAD (very long chain acyl CoA dehydrogenase deficiency) E71.310
- zinc, dietary E60
Index entries, exactly as the book files them. This says they are listed together — not that any of them is documented in your chart.
Billable FY2027 2026-10-01 → 2027-09-30
FY2026–2027 only
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Instructional notes8
QA0code
Code also
- , if applicable, any associated conditions, such as:
- attention-deficit hyperactivity disorders (F90.-)F90.-
- autism spectrum disorder (F84.0)F84.0
- developmental and epileptic encephalopathy (G93.45)G93.45
- epilepsy, by specific type (G40.-)G40.-
- intellectual disabilities (F70-F79)F70-F79
- pervasive developmental disorders (F84.-)F84.-
QA0.0131code
Inclusion terms
- GABA transporter 1 deficiency
Official Guidelines
No guideline section names this code or its chapter.
Index entries leading here2
Alongside this code1same parent — QA0.013
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.