(F01 – F99)
F60.2
BookmarkAntisocial personality 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.
How to use this page
Everything the published sources say about one code, on one page.
- Read the Excludes1 block first — it is the one that stops you coding this at all alongside another code.
- Excludes2, Code first, Use additional and Includes follow. A note inherited from a parent category is labelled with the category it came from, so you can see why it applies.
- Official Guidelines sit below. "Guidelines naming this code" cite the code or a range containing it; "Chapter guidance" is the general guidance for its chapter and is the weaker signal.
- Guideline text is quoted verbatim with its section number and page, so you can check it against the published document.
- Risk-model chips show which published CMS models map this code.
What this page does not do
- Guidance is quoted, never paraphrased — a paraphrase of a coding rule is a different rule.
- Medication candidates, where shown, are matched by condition *name* and are offered as candidates for you to judge. They are not "the drugs for this code".
Exclusions3never code together
- symptoms, signs and abnormal clinical laboratory findings, not elsewhere classified (R00-R99)R00-R99
Excludes1 — never code together. The excluded condition and this one are mutually exclusive.
Excludes2 — not included here, but the patient may have both. Code both when documented.
Instructional notes6
Official Guidelines10names this code
ICD-10-CM Official Guidelines for Coding and Reporting, quoted in full. Published by CMS and NCHS; in the public domain.
Assign code F45.41, for pain that is exclusively related to psychological disorders. As indicated by the Excludes 1 note under category G89, a code from category G89 should not be assigned with code F45.41. Code F45.42, Pain disorders with related psychological factors, should be used with a code from category G89, Pain, not elsewhere classified, if there is documentation of a psychological component for a patient with acute or chronic pain. See Section I.C.6. Pain
use
Selection of codes describing “in remission” for categories F10-F19, Mental and behavioral disorders due to psychoactive substance use (categories F10-F19 with -.11, -.21, -.91) requires the provider’s clinical judgment and are assigned only on the basis of provider documentation (as defined in the Official Guidelines for Coding and Reporting), unless otherwise instructed by the classification. Mild substance use disorders in early or sustained remission are classified to the appropriate codes for substance abuse in remission, and moderate or severe substance use disorders in early or sustained remission are classified to the appropriate codes for substance dependence in remission.
When the provider documentation refers to use, abuse and dependence of the same substance (e.g. alcohol, opioid, cannabis, etc.), only one code should be assigned to identify the pattern of use based on the following hierarchy: • If both use and abuse are documented, assign only the code for abuse • If both abuse and dependence are documented, assign only the code for dependence • If use, abuse and dependence are all documented, assign only the code for dependence • If both use and dependence are documented, assign only the code for dependence.
As with all other unspecified diagnoses, the codes for unspecified psychoactive substance use (F10.9-, F11.9-, F12.9-, F13.9-, F14.9-, F15.9-, F16.9-, F18.9-, F19.9-) should only be assigned based on provider documentation and when they meet the definition of a reportable diagnosis (see Section III, Reporting Additional Diagnoses). These codes are to be used only when the psychoactive substance use is associated with a substance related disorder (chapter 5 disorders such as sexual dysfunction, sleep disorder, or a mental or behavioral disorder) or medical condition, and such a relationship is documented by the provider.
and Dependence Medical conditions due to substance use, abuse, and dependence are not classified as substance-induced disorders. Assign the diagnosis code for the medical condition as directed by the Alphabetical Index along with the appropriate psychoactive substance use, abuse or dependence code. For example, for alcoholic pancreatitis due to alcohol dependence, assign the appropriate code from subcategory K85.2, Alcohol induced acute pancreatitis, and the appropriate code from subcategory F10.2, such as code F10.20, Alcohol dependence, uncomplicated. It would not be appropriate to assign code F10.288, Alcohol dependence with other alcohol-induced disorder.
A code from category Y90, Evidence of alcohol involvement determined by blood alcohol level, may be assigned when this information is documented and the patient’s provider has documented a condition classifiable to category F10, Alcohol related disorders. The blood alcohol level does not need to be documented by the patient’s provider in order for it to be coded. See Section I.B.14. for blood alcohol level documentation by clinicians other than patient's provider.
Factitious disorder imposed on self or Munchausen’s syndrome is a disorder in which a person falsely reports or causes his or her own physical or psychological signs or symptoms. For patients with documented factitious disorder on self or Munchausen’s syndrome, assign the appropriate code from subcategory F68.1-, Factitious disorder imposed on self. Munchausen’s syndrome by proxy (MSBP) is a disorder in which a caregiver (perpetrator) falsely reports or causes an illness or injury in another person (victim) under his or her care, such as a child, an elderly adult, or a person who has a disability. The condition is also referred to as “factitious disorder imposed on another” or “factitious disorder by proxy.” The perpetrator, not the victim, receives this diagnosis. Assign code F68.A, Factitious disorder imposed on another, to the perpetrator’s record. For the victim of a patient suffering from MSBP, assign the appropriate code from categories T74, Adult and child abuse, neglect and other maltreatment, confirmed, or T76, Adult and child abuse, neglect and other maltreatment, suspected. See Section I.C.19.f. Adult and child abuse, neglect and other maltreatment
The ICD-10-CM classifies dementia (categories F01, F02, and F03) on the basis of the etiology and severity (unspecified, mild, moderate or severe). Selection of the appropriate severity level requires the provider’s clinical judgment and codes should be assigned only on the basis of provider documentation (as defined in the Official Guidelines for Coding and Reporting), unless otherwise instructed by the classification. If the documentation does not provide information about the severity of the dementia, assign the appropriate code for unspecified severity. If a patient is admitted to an inpatient acute care hospital or other inpatient facility setting with dementia at one severity level and it progresses to a higher severity level, assign one code for the highest severity level reported during the stay.
Index entries leading here11
- Disorder (of) — see also Disease
- Personality (disorder) F60.9
- Antisocial personality F60.2
- Asocial personality F60.2
- Criminalism F60.2
- Deficiency, deficient
- moral F60.2
- Disturbance (s) — see also Disease
- sociopathic F60.2
- Liar, pathologic F60.2
- Mendacity, pathologic F60.2
- State (of)
- psychopathic (constitutional) F60.2
- Psychopathy, psychopathic
- state F60.2
Alongside this code9same parent — F60
Additional references
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.