See Section I.C.21. Factors influencing health status and contact with health services, Screening Appendix I Present on Admission Reporting Guidelines Introduction These guidelines are to be used as a supplement to the ICD-10-CM Official Guidelines for Coding and Reporting to facilitate the assignment of the Present on Admission (POA) indicator for each diagnosis and external cause of injury code reported on claim forms (UB-04 and 837 Institutional). These guidelines are not intended to replace any guidelines in the main body of the ICD-10-CM Official Guidelines for Coding and Reporting. The POA guidelines are not intended to provide guidance on when a condition should be coded, but rather, how to apply the POA indicator to the final set of diagnosis codes that have been assigned in accordance with Sections I, II, and III of the official coding guidelines. Subsequent to the assignment of the ICD-10-CM codes, the POA indicator should then be assigned to those conditions that have been coded. As stated in the Introduction to the ICD-10-CM Official Guidelines for Coding and Reporting, a joint effort between the healthcare provider and the coder is essential to achieve complete and accurate documentation, code assignment, and reporting of diagnoses and procedures. The importance of consistent, complete documentation in the medical record cannot be overemphasized. Medical record documentation from any provider involved in the care and treatment of the patient may be used to support the determination of whether a condition was present on admission or not. In the context of the official coding guidelines, the term “provider” means a physician or any qualified healthcare practitioner who is legally accountable for establishing the patient’s diagnosis. These guidelines are not a substitute for the provider’s clinical judgment as to the determination of whether a condition was/was not present on admission. The provider should be queried regarding issues related to the linking of signs/symptoms, timing of test results, and the timing of findings. Please see the CDC website for the detailed list of ICD-10-CM codes that do not require the use of a POA indicator (https://www.cdc.gov/nchs/icd/icd-10-cm/files.html). The codes and categories on this exempt list are for circumstances regarding the healthcare encounter or factors influencing health status that do not represent a current disease or injury or that describe conditions that are always present on admission. General Reporting Requirements All claims involving inpatient admissions to general acute care hospitals or other facilities that are subject to a law or regulation mandating collection of present on admission information. Present on admission is defined as present at the time the order for inpatient admission occurs -- conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered as present on admission. POA indicator is assigned to principal and secondary diagnoses (as defined in Section II of the Official Guidelines for Coding and Reporting) and the external cause of injury codes. Issues related to inconsistent, missing, conflicting or unclear documentation must still be resolved by the provider. If a condition would not be coded and reported based on UHDDS definitions and current official coding guidelines, then the POA indicator would not be reported. Reporting Options Y – Yes N – No U – Unknown W – Clinically undetermined Unreported/Not used – (Exempt from POA reporting) Reporting Definitions Y = present at the time of inpatient admission N = not present at the time of inpatient admission U = documentation is insufficient to determine if condition is present on admission W = provider is unable to clinically determine whether condition was present on admission or not Timeframe for POA Identification and Documentation There is no required timeframe as to when a provider (per the definition of “provider” used in these guidelines) must identify or document a condition to be present on admission. In some clinical situations, it may not be possible for a provider to make a definitive diagnosis (or a condition may not be recognized or reported by the patient) for a period of time after admission. In some cases, it may be several days before the provider arrives at a definitive diagnosis. This does not mean that the condition was not present on admission. Determination of whether the condition was present on admission or not will be based on the applicable POA guideline as identified in this document, or on the provider’s best clinical judgment. If at the time of code assignment the documentation is unclear as to whether a condition was present on admission or not, it is appropriate to query the provider for clarification. Assigning the POA Indicator Condition is on the “Exempt from Reporting” list Leave the “present on admission” field blank if the condition is on the list of ICD- 10-CM codes for which this field is not applicable. This is the only circumstance in which the field may be left blank. POA Explicitly Documented Assign Y for any condition the provider explicitly documents as being present on admission. Assign N for any condition the provider explicitly documents as not present at the time of admission. Conditions diagnosed prior to inpatient admission Assign “Y” for conditions that were diagnosed prior to admission (example: hypertension, diabetes mellitus, asthma) Conditions diagnosed during the admission but clearly present before admission Assign “Y” for conditions diagnosed during the admission that were clearly present but not diagnosed until after admission occurred. Diagnoses subsequently confirmed after admission are considered present on admission if at the time of admission they are documented as suspected, possible, rule out, differential diagnosis, or constitute an underlying cause of a symptom that is present at the time of admission. Condition develops during outpatient encounter prior to inpatient admission Assign Y for any condition that develops during an outpatient encounter prior to a written order for inpatient admission. Documentation does not indicate whether condition was present on admission Assign “U” when the medical record documentation is unclear as to whether the condition was present on admission. “U” should not be routinely assigned and used only in very limited circumstances. Coders are encouraged to query the providers when the documentation is unclear. Documentation states that it cannot be determined whether the condition was or was not present on admission Assign “W” when the medical record documentation indicates that it cannot be clinically determined whether or not the condition was present on admission. Chronic condition with acute exacerbation during the admission If a single code identifies both the chronic condition and the acute exacerbation, see POA guidelines pertaining to codes that contain multiple clinical concepts. If a single code only identifies the chronic condition and not the acute exacerbation (e.g., acute exacerbation of chronic leukemia), assign “Y.” Conditions documented as possible, probable, suspected, or rule out at the time of discharge If the final diagnosis contains a possible, probable, suspected, or rule out diagnosis, and this diagnosis was based on signs, symptoms or clinical findings suspected at the time of inpatient admission, assign “Y.” If the final diagnosis contains a possible, probable, suspected, or rule out diagnosis, and this diagnosis was based on signs, symptoms or clinical findings that were not present on admission, assign “N”. Conditions documented as impending or threatened at the time of discharge If the final diagnosis contains an impending or threatened diagnosis, and this diagnosis is based on symptoms or clinical findings that were present on admission, assign “Y”. If the final diagnosis contains an impending or threatened diagnosis, and this diagnosis is based on symptoms or clinical findings that were not present on admission, assign “N”. Acute and Chronic Conditions Assign “Y” for acute conditions that are present at time of admission and N for acute conditions that are not present at time of admission. Assign “Y” for chronic conditions, even though the condition may not be diagnosed until after admission. If a single code identifies both an acute and chronic condition, see the POA guidelines for codes that contain multiple clinical concepts. Codes That Contain Multiple Clinical Concepts Assign “N” if at least one of the clinical concepts included in the code was not present on admission (e.g., COPD with acute exacerbation and the exacerbation was not present on admission; gastric ulcer that does not start bleeding until after admission; asthma patient develops status asthmaticus after admission). Assign “Y” if all of the clinical concepts included in the code were present on admission (e.g., duodenal ulcer that perforates prior to admission). For infection codes that include the causal organism, assign “Y” if the infection (or signs of the infection) were present on admission, even though the culture results may not be known until after admission (e.g., patient is admitted with pneumonia and the provider documents Pseudomonas as the causal organism a few days later). Same Diagnosis Code for Two or More Conditions When the same ICD-10-CM diagnosis code applies to two or more conditions during the same encounter (e.g., two separate conditions classified to the same ICD-10-CM diagnosis code): Assign “Y” if all conditions represented by the single ICD-10-CM code were present on admission (e.g., bilateral unspecified age-related cataracts). Assign “N” if any of the conditions represented by the single ICD-10-CM code was not present on admission (e.g. traumatic secondary and recurrent hemorrhage and seroma is assigned to a single code T79.2, but only one of the conditions was present on admission). Obstetrical conditions Whether or not the patient delivers during the current hospitalization does not affect assignment of the POA indicator. The determining factor for POA assignment is whether the pregnancy complication or obstetrical condition described by the code was present at the time of admission or not. If the pregnancy complication or obstetrical condition was present on admission (e.g., patient admitted in preterm labor), assign “Y”. If the pregnancy complication or obstetrical condition was not present on admission (e.g., 2 degree laceration during delivery, postpartum hemorrhage that occurred during current hospitalization, fetal distress develops after admission), assign “N”. If the obstetrical code includes more than one diagnosis and any of the diagnoses identified by the code were not present on admission assign “N”. (e.g., Category O11, Pre-existing hypertension with pre-eclampsia) Perinatal conditions Newborns are not considered to be admitted until after birth. Therefore, any condition present at birth or that developed in utero is considered present at admission and should be assigned “Y”. This includes conditions that occur during delivery (e.g., injury during delivery, meconium aspiration, exposure to streptococcus B in the vaginal canal). Congenital conditions and anomalies Assign “Y” for congenital conditions and anomalies except for categories Q00- Q99, Congenital anomalies, which are on the exempt list. Congenital conditions are always considered present on admission. External cause of injury codes Assign “Y” for any external cause code representing an external cause of morbidity that occurred prior to inpatient admission (e.g., patient fell out of bed at home, patient fell out of bed in emergency room prior to admission) Assign “N” for any external cause code representing an external cause of morbidity that occurred during inpatient hospitalization (e.g., patient fell out of hospital bed during hospital stay, patient experienced an adverse reaction to a medication administered after inpatient admission).
Q80.9
BookmarkCongenital ichthyosis, unspecified
Filed alongside this entry 585
under Disease, diseased
- absorbent system I87.8
- acid-peptic K30
- Acosta's T70.29
- Adams-Stokes (-Morgagni) (syncope with heart block) I45.9
- Addison's anemia (pernicious) D51.0
- adenoids (and tonsils) J35.9
- adrenal (capsule) (cortex) (gland) (medullary) E27.9
- ainhum L94.6
- akamushi (scrub typhus) A75.3
- Albers-Schönberg (marble bones) Q78.2
- Alexander G31.86
- alimentary canal K63.9
- alligator-skin Q80.9
- alpha heavy chain C88.3
- alpine T70.29
- altitude T70.20
- alveoli, teeth K08.9
- Alzheimer's G30.9
- Andersen's (glycogenosis IV) E74.09
- Andes T70.29
- Andrews' (bacterid) L08.89
- angiospastic I73.9
- antiglomerular basement membrane (anti- GBM) antibody M31.0
- Antopol E74.05
- anus K62.9
- aorta (nonsyphilitic) I77.9
- aortic (heart) (valve) I35.9
- Apollo B30.3
- appendix K38.9
- aqueous (chamber) H21.9
- arterial I77.9
- arteriolar (generalized) (obliterative) I77.9
- artery I77.9
- arthropod-borne NOS (viral) A94
- atticoantral, chronic H66.20
- Australian X A83.4
- autoimmune (systemic) NOS M35.9
- autoinflammatory M04.9
- Ayerza's (pulmonary artery sclerosis with pulmonary hypertension) I27.0
- Babington's (familial hemorrhagic telangiectasia) I78.0
- bacterial A49.9
- Baelz's (cheilitis glandularis apostematosa) K13.0
- bagasse J67.1
- Bang's (brucella abortus) A23.1
- Bannister's T78.3
- Barraquer (-Simons') (progressive lipodystrophy) E88.11
- Bartholin's gland N75.9
- basal ganglia G25.9
- Bateman's B08.1
- Batten-Steinert G71.11
- Battey A31.0
- Beard's (neurasthenia) F48.8
- behavioral, organic F07.9
- Beigel's (white piedra) B36.2
- Bernard-Soulier (thrombopathy) D69.19
- Biermer's (pernicious anemia) D51.0
- bile duct (common) (hepatic) K83.9
- biliary (tract) K83.9
- bird fancier's J67.2
- black lung J60
- bladder N32.9
- bleeder's D66
- blood D75.9
- Blount M92.51
- Bodechtel-Guttmann (subacute sclerosing panencephalitis) A81.1
- bone-marrow D75.9
- Borna A83.9
- Bornholm (epidemic pleurodynia) B33.0
- Bouchard's (myopathic dilatation of the stomach) K31.0
- Bouillaud's (rheumatic heart disease) I01.9
- Bourneville (-Brissaud) (tuberous sclerosis) Q85.1
- Bouveret (-Hoffmann) (paroxysmal tachycardia) I47.9
- bowel K63.9
- brain G93.9
- breast N64.9
- Bretonneau's (diphtheritic malignant angina) A36.0
- Brill's (recrudescent typhus) A75.1
- Brill-Zinsser (recrudescent typhus) A75.1
- Brocq-Duhring (dermatitis herpetiformis) L13.0
- bronchopulmonary J98.4
- bronchus NEC J98.09
- bronze Addison's E27.1
- budgerigar fancier's J67.2
- bullous L13.9
- Buerger's (thromboangiitis obliterans) I73.1
- Bürger-Grütz (essential familial hyperlipemia) E78.3
- caisson T70.3
- Canavan E75.28
- capillaries I78.9
- Carapata A68.0
- carcinoid E34.00
- cardiopulmonary, chronic I27.9
- cardiovascular (atherosclerotic) I25.10
- Castellani's A69.8
- Castleman (unicentric) (multicentric) D47.Z2
- cat-scratch A28.1
- Cavare's (familial periodic paralysis) G72.3
- cecum K63.9
- celiac (adult) (infantile) (with steatorrhea) K90.0
- cellular tissue L98.9
- central core G71.29
- cerebrospinal G96.9
- cerebrovascular I67.9
- cervix (uteri) (noninflammatory) N88.9
- Chabert's A22.9
- Chédiak-Steinbrinck (-Higashi) (congenital gigantism of peroxidase granules) E70.330
- chest J98.9
- Chiari's (hepatic vein thrombosis) I82.0
- Chicago B40.9
- Chignon B36.8
- chigo, chigoe B88.1
- childhood granulomatous D71.8
- Chinese liver fluke B66.1
- chlamydial A74.9
- cholecystic K82.9
- choroid H31.9
- Christmas D67
- chronic bullous of childhood L12.2
- chylomicron retention E78.3
- ciliary body H21.9
- circulatory (system) NEC I99.8
- collagen NOS (nonvascular) (vascular) M35.9
- colon K63.9
- colonic inflammatory bowel, unclassified (IBDU) K52.3
- compressed air T70.3
- Concato's (pericardial polyserositis) A19.9
- conjunctiva H11.9
- connective tissue, systemic (diffuse) M35.9
- Conor and Bruch's (boutonneuse fever) A77.1
- Cori's (glycogenosis III) E74.03
- corkhandler's or corkworker's J67.3
- cornea H18.9
- corpus cavernosum N48.9
- COVID-19 U07.1
- coxsackie (virus) NEC B34.1
- cranial nerve NOS G52.9
- Crocq's (acrocyanosis) I73.89
- Curschmann G71.11
- cytomegalic inclusion (generalized) B25.9
- cytomegaloviral B25.9
- Daae (-Finsen) (epidemic pleurodynia) B33.0
- Danon E74.05
- Débove's (splenomegaly) R16.1
- Degos' I77.89
- demyelinating, demyelinizating (nervous system) G37.9
- dense deposit N05.6
- de Quervain's (tendon sheath) M65.4
- Devergie's (pityriasis rubra pilaris) L44.0
- Devic's G36.0
- diaphorase deficiency D74.0
- diaphragm J98.6
- diarrheal, infectious NEC A09
- digestive system K92.9
- Dubois (thymus) A50.59
- Duchenne-Griesinger G71.01
- ductless glands E34.9
- Duhring's (dermatitis herpetiformis) L13.0
- duodenum K31.9
- Dupré's (meningism) R29.1
- Dupuytren's (muscle contracture) M72.0
- Durand-Nicholas-Favre (climatic bubo) A55
- Duroziez's (congenital mitral stenosis) Q23.2
- Ebola (virus) A98.4
- Ebstein's heart Q22.5
- echovirus NEC B34.1
- Eddowes' (brittle bones and blue sclera) Q78.0
- edentulous (alveolar) ridge K06.9
- Edsall's T67.2
- Eichstedt's (pityriasis versicolor) B36.0
- Eisenmenger's (irreversible) I27.83
- Ellis-van Creveld (chondroectodermal dysplasia) Q77.6
- end stage renal (ESRD) N18.6
- endocrine glands or system NEC E34.9
- endomyocardial (eosinophilic) I42.3
- English (rickets) E55.0
- enteroviral, enterovirus NEC B34.1
- epidemic B99.9
- epididymis N50.9
- Erb (-Landouzy) G71.02
- Erdheim-Chester (ECD) E88.89
- esophagus K22.9
- Eulenburg's (congenital paramyotonia) G71.19
- extrapyramidal G25.9
- eye H57.9
- eyeball H44.9
- eyeworm of Africa B74.3
- facial nerve (seventh) G51.9
- Fahr (of brain) G23.8
- fallopian tube (noninflammatory) N83.9
- familial periodic paralysis G72.3
- Fanconi ('s) D61.03
- Favre-Durand-Nicolas (climatic bubo) A55
- Fede's K14.0
- female pelvic inflammatory N73.9
- Fernels' (aortic aneurysm) I71.9
- Fiedler's (leptospiral jaundice) A27.0
- fifth B08.3
- fish-skin Q80.9
- flax-dresser's J66.1
- foot and mouth B08.8
- foot process N04.9
- Forbes' (glycogenosis III) E74.03
- Fordyce-Fox (apocrine miliaria) L75.2
- Fordyce's (ectopic sebaceous glands) (mouth) Q38.6
- Forestier's (rhizomelic pseudopolyarthritis) M35.3
- Fournier (gangrene) N49.3
- fourth B08.8
- Fox (-Fordyce) (apocrine miliaria) L75.2
- Franklin C88.2
- Frei's (climatic bubo) A55
- fungus NEC B49
- Gaisböck's (polycythemia hypertonica) D75.1
- gallbladder K82.9
- gamma heavy chain C88.2
- Gamna's (siderotic splenomegaly) D73.2
- Gamstorp's (adynamia episodica hereditaria) G72.3
- Gandy-Nanta (siderotic splenomegaly) D73.2
- ganister J62.8
- gastroesophageal reflux (GERD) K21.9
- gastrointestinal (tract) K92.9
- Gee (-Herter) (-Heubner) (-Thaysen) (nontropical sprue) K90.0
- Gerhardt's (erythromelalgia) I73.81
- Gibert's (pityriasis rosea) L42
- Gierke's (glycogenosis I) E74.01
- Gilles de la Tourette's (motor-verbal tic) F95.2
- gingiva K06.9
- gland (lymph) I89.9
- Glanzmann's (hereditary hemorrhagic thrombasthenia) D69.11
- globe H44.9
- glycogen storage E74.00
- Goldstein's (familial hemorrhagic telangiectasia) I78.0
- gonococcal NOS A54.9
- graft-versus-host (GVH) D89.813
- grainhandler's J67.8
- granulomatous (childhood) (chronic) D71.8
- Grisel's M43.6
- Gruby's (tinea tonsurans) B35.0
- Guillain-Barré G61.0
- Guinon's (motor-verbal tic) F95.2
- gum K06.9
- gynecological N94.9
- H (Hartnup's) E72.02
- Hageman (congenital factor XII deficiency) D68.2
- hair (color) (shaft) L67.9
- Hamman's (spontaneous mediastinal emphysema) J98.2
- hand, foot and mouth B08.4
- Hantavirus, with pulmonary manifestations B33.4
- Harada's H30.81
- Hartnup (pellagra-cerebellar ataxia-renal aminoaciduria) E72.02
- Hart's (pellagra-cerebellar ataxia-renal aminoaciduria) E72.02
- Hashimoto's (struma lymphomatosa) E06.3
- heart (organic) I51.9
- Heartland A93.8
- heavy chain NEC C88.2
- hematopoietic organs D75.9
- hemolytic (newborn) P55.9
- hemorrhagic D69.9
- Henoch (-Schönlein) (purpura nervosa) D69.0
- hepatobiliary K83.9
- hepatolenticular E83.01
- herpesviral, disseminated B00.7
- Hers' (glycogenosis VI) E74.09
- Herter (-Gee) (-Heubner) (nontropical sprue) K90.0
- Heubner-Herter (nontropical sprue) K90.0
- high fetal gene or hemoglobin thalassemia D56.9
- hip (joint) M25.9
- His (-Werner) (trench fever) A79.0
- Hodgson's I71.20
- hookworm B76.9
- host-versus-graft D89.813
- human immunodeficiency virus (HIV) B20
- Huntington's G10
- Hunt's (herpetic geniculate ganglionitis) (neuralgia) B02.21
- hydroxyapatite deposition M11.00
- hypophysis E23.7
- Iceland G93.39
- I-cell E77.0
- IgG4-related D89.84
- immune D89.9
- immunoproliferative (malignant) C88.9
- inclusion B25.9
- infectious, infective B99.9
- intestine K63.9
- iris H21.9
- iron metabolism or storage E83.10
- island (scrub typhus) A75.3
- jaw M27.9
- jigger B88.1
- Jourdain's (acute gingivitis) K05.00
- Kaschin-Beck (endemic polyarthritis) M12.10
- Katayama B65.2
- Kedani (scrub typhus) A75.3
- Keshan E59
- kidney (functional) (pelvis) N28.9
- Kimura D21.9
- Kinnier Wilson's (hepatolenticular degeneration) E83.01
- Klippel-Feil (brevicollis) Q76.1
- Kok Q89.89
- Korsakoff's (nonalcoholic) F04
- Kostmann's (infantile genetic agranulocytosis) D70.0
- kuru A81.81
- Kyasanur Forest A98.2
- Lafora body G40.C09
- Lancereaux-Mathieu (leptospiral jaundice) A27.0
- Landry's G61.0
- Larrey-Weil (leptospiral jaundice) A27.0
- larynx J38.7
- Ledderhose M72.2
- legionnaires' A48.1
- Lenegre's I44.2
- lens H27.9
- Lev's (acquired complete heart block) I44.2
- Lewy body (dementia) G31.83
- Lichtheim's (subacute combined sclerosis with pernicious anemia) D51.0
- Lightwood's (renal tubular acidosis) N25.89
- Lignac's (cystinosis) E72.04
- lip K13.0
- lipid-storage E75.6
- Lipschütz's N76.6
- liver (chronic) (organic) K76.9
- Lobo's (keloid blastomycosis) B48.0
- Lobstein's (brittle bones and blue sclera) Q78.0
- Ludwig's (submaxillary cellulitis) K12.2
- lumbosacral region M53.87
- lung J98.4
- Lutembacher's (atrial septal defect with mitral stenosis) Q21.19
- Lyme A69.20
- lymphatic (gland) (system) (channel) (vessel) I89.9
- lymphoproliferative D47.9
- Magitot's M27.2
- Manson's B65.1
- maple bark J67.6
- maple-syrup-urine E71.0
- Marburg (virus) A98.3
- Marion's (bladder neck obstruction) N32.0
- Mathieu's (leptospiral jaundice) A27.0
- Maxcy's A75.2
- McArdle (-Schmid-Pearson) (glycogenosis V) E74.04
- mediastinum J98.59
- medullary center (idiopathic) (respiratory) G93.89
- Meige's (chronic hereditary edema) Q82.0
- mental F99
- mesenchymal M35.9
- mesenteric embolic K55.039
- metabolic, metabolism E88.9
- metal-polisher's J62.8
- metastatic C79.9
- Mikulicz' (dryness of mouth, absent or decreased lacrimation) K11.8
- Milroy's (chronic hereditary edema) Q82.0
- minicore G71.29
- Minor's G95.19
- Minot's (hemorrhagic disease, newborn) P53
- Mitchell's (erythromelalgia) I73.81
- mitral (valve) I05.9
- mixed connective tissue M35.1
- MOG antibody G37.81
- moldy hay J67.0
- Monge's T70.29
- Morgagni-Adams-Stokes (syncope with heart block) I45.9
- Morgagni's (syndrome) (hyperostosis frontalis interna) M85.2
- Morvan's G60.8
- motor neuron (bulbar) (mixed type) (spinal) G12.20
- moyamoya I67.5
- mu heavy chain disease C88.2
- multicore G71.29
- multiminicore G71.29
- mushroom workers' J67.5
- mycotic B49
- myelin oligodendrocyte glycoprotein antibody G37.81
- myelodysplastic C94.6
- myelodysplastic/myeloproliferative neoplasm, unclassifiable C94.6
- myeloproliferative D47.1
- myocardium, myocardial I51.5
- myoneural G70.9
- Naegeli's Q82.8
- nails L60.9
- Nairobi (sheep virus) A93.8
- nasal J34.9
- nemaline body G71.21
- nervous system G98.8
- neuromuscular system G70.9
- Newcastle B30.8
- Nicolas (-Durand)-Favre (climatic bubo) A55
- nipple N64.9
- Nishimoto (-Takeuchi) I67.5
- nonarthropod-borne NOS (viral) B34.9
- nonautoimmune hemolytic D59.4
- Nonne-Milroy-Meige (chronic hereditary edema) Q82.0
- nose J34.9
- nutritional E63.9
- oast-house-urine E72.19
- obliterative vascular I77.1
- Opitz's (congestive splenomegaly) D73.2
- Oriental liver fluke B66.1
- Oriental lung fluke B66.4
- Ormond's N13.5
- Oropouche virus A93.0
- Osler-Rendu (familial hemorrhagic telangiectasia) I78.0
- osteofibrocystic E21.0
- Otto's M24.7
- ovary (noninflammatory) N83.9
- p110d-activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency [PASLI] D81.82
- pancreas K86.9
- panvalvular I08.9
- parametrium (noninflammatory) N83.9
- parasitic B89
- parathyroid (gland) E21.5
- Parkinson's G20.A1
- parodontal K05.6
- Parrot's (syphilitic osteochondritis) A50.02
- Paxton's (white piedra) B36.2
- pelvis, pelvic K6A.8
- penis N48.9
- periapical tissues NOS K04.90
- periodontal K05.6
- peritoneum K66.9
- persistent mucosal (middle ear) H66.20
- pharynx J39.2
- photochromogenic (acid-fast bacilli) (pulmonary) A31.0
- Pick's G31.01
- pigeon fancier's J67.2
- pineal gland E34.8
- Pinkus' (lichen nitidus) L44.1
- pinworm B80
- Piry virus A93.8
- pituitary (gland) E23.7
- pituitary-snuff-taker's J67.8
- pleura (cavity) J94.9
- pneumatic drill (hammer) T75.21
- Pollitzer's (hidradenitis suppurativa) L73.2
- polyethylene T84.05
- Pompe's (glycogenosis II) E74.02
- Posadas-Wernicke B38.9
- prepuce N47.8
- Pringle's (tuberous sclerosis) Q85.1
- prion, central nervous system A81.9
- prostate N42.9
- protozoal B64
- pseudo-Hurler's E77.0
- psychiatric F99
- Puente's (simple glandular cheilitis) K13.0
- puerperal O90.89
- pulp (dental) NOS K04.90
- pulseless M31.4
- Putnam's (subacute combined sclerosis with pernicious anemia) D51.0
- Pyle (-Cohn) (metaphyseal dysplasia) Q78.5
- ragpicker's or ragsorter's A22.1
- rectum K62.9
- Refsum's (heredopathia atactica polyneuritiformis) G60.1
- renal (functional) (pelvis) N28.9
- Rendu-Osler-Weber (familial hemorrhagic telangiectasia) I78.0
- respiratory (tract) J98.9
- retina, retinal H35.9
- rickettsial NOS A79.9
- Riga (-Fede) (cachectic aphthae) K14.0
- Ritter's L00
- Rivalta's (cervicofacial actinomycosis) A42.2
- Robles' (onchocerciasis) B73.01
- rod body G71.21
- Roger's (congenital interventricular septal defect) Q21.0
- Rosenthal's (factor XI deficiency) D68.1
- Rossbach's (hyperchlorhydria) K31.89
- Ross River B33.1
- Runeberg's (progressive pernicious anemia) D51.0
- sacroiliac NEC M53.3
- salivary gland or duct K11.9
- sandworm B76.9
- Schönlein (-Henoch) (purpura rheumatica) D69.0
- Schwalbe-Ziehen-Oppenheim G24.1
- Schwartz-Jampel G71.13
- sclera H15.9
- scrofulous (tuberculous) A18.2
- scrotum N50.9
- sebaceous glands L73.9
- seminal vesicle N50.9
- serum NEC T80.69
- sexually transmitted A64
- Sézary C84.1
- shimamushi (scrub typhus) A75.3
- shipyard B30.0
- sickle-cell D57.1
- silo-filler's J68.8
- simian B B00.4
- Simons' (progressive lipodystrophy) E88.11
- sin nombre virus B33.4
- Sirkari's B55.0
- sixth B08.20
- skin L98.9
- slim (HIV) B20
- small vessel I73.9
- Sneddon-Wilkinson (subcorneal pustular dermatosis) L13.1
- South African creeping B88.09
- spinal (cord) G95.9
- spinocerebellar (hereditary) G11.9
- spleen D73.9
- Startle Q89.89
- Steinert's G71.11
- Sticker's (erythema infectiosum) B08.3
- Stokes-Adams (syncope with heart block) I45.9
- stomach K31.9
- stonemason's J62.8
- striatopallidal system NEC G25.89
- Stuart-Prower (congenital factor X deficiency) D68.2
- Stuart's (congenital factor X deficiency) D68.2
- supporting structures of teeth K08.9
- suprarenal (capsule) (gland) E27.9
- sweat glands L74.9
- Sweeley-Klionsky E75.21
- swimming-pool granuloma A31.1
- Sylvest's (epidemic pleurodynia) B33.0
- sympathetic nervous system G90.9
- systemic tissue mast cell D47.02
- tanapox (virus) B08.71
- Tangier E78.6
- Tarral-Besnier (pityriasis rubra pilaris) L44.0
- Tauri's E74.09
- terminal vessel I73.9
- testis N50.9
- Thaysen-Gee (nontropical sprue) K90.0
- Thomsen G71.12
- throat J39.2
- thymus (gland) E32.9
- thyroid (gland) E07.9
- Tietze's M94.0
- tongue K14.9
- tonsils, tonsillar (and adenoids) J35.9
- tooth, teeth K08.9
- Tourette's F95.2
- trachea NEC J39.8
- tricuspid I07.9
- triglyceride-storage E75.5
- tsutsugamushi A75.3
- tube (fallopian) (noninflammatory) N83.9
- tubo-ovarian (noninflammatory) N83.9
- tubulo-interstitial N15.9
- Uhl's Q24.8
- Underwood's (sclerema neonatorum) P83.0
- ureter N28.9
- urethra N36.9
- urinary (tract) N39.9
- uterus (noninflammatory) N85.9
- uveal tract (anterior) H21.9
- vagabond's B85.1
- vagina, vaginal (noninflammatory) N89.9
- valve, valvular I38
- van Creveld-von Gierke (glycogenosis I) E74.01
- vas deferens N50.9
- vascular I99.9
- vasomotor I73.9
- vasospastic I73.9
- vein I87.9
- venereal A64
- viral, virus B34.9
- vitreous H43.9
- vocal cord J38.3
- Volkmann's, acquired T79.6
- von Eulenburg's (congenital paramyotonia) G71.19
- von Gierke's (glycogenosis I) E74.01
- von Willebrand (-Jürgens) (angiohemophilia) D68.00
- Vrolik's (osteogenesis imperfecta) Q78.0
- vulva (noninflammatory) N90.9
- Wallgren's (obstruction of splenic vein with collateral circulation) I87.8
- Wassilieff's (leptospiral jaundice) A27.0
- wasting NEC E88.A
- Waterhouse-Friderichsen A39.1
- Wegner's (syphilitic osteochondritis) A50.02
- Weil's (leptospiral jaundice of lung) A27.0
- Weir Mitchell's (erythromelalgia) I73.81
- Werdnig-Hoffmann G12.0
- Wermer's E31.21
- Werner-His (trench fever) A79.0
- Werner-Schultz (neutropenic splenomegaly) D73.81
- Wernicke-Posadas B38.9
- whipworm B79
- white blood cells D72.9
- white matter R90.82
- white-spot, meaning lichen sclerosus et atrophicus L90.0
- Wilkie's K55.1
- Wilkinson-Sneddon (subcorneal pustular dermatosis) L13.1
- Wilson's (hepatolenticular degeneration) E83.01
- woolsorter's A22.1
- yaba monkey tumor B08.72
- yaba pox (virus) B08.72
- Zika virus A92.5
- zoonotic, bacterial A28.9
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".
Exclusions1never code together
Instructional notes
No further instructional notes apply.
Official Guidelines2names this code
ICD-10-CM Official Guidelines for Coding and Reporting, quoted in full. Published by CMS and NCHS; in the public domain.
Assign an appropriate code(s) from categories Q00-QA1, Congenital malformations, deformations, and chromosomal abnormalities when a malformation/deformation or chromosomal abnormality is documented. A malformation/deformation/or chromosomal abnormality may be the principal/first-listed diagnosis on a record or a secondary diagnosis. When a malformation/deformation or chromosomal abnormality does not have a unique code assignment, assign additional code(s) for any manifestations that may be present. When the code assignment specifically identifies the malformation/deformation or chromosomal abnormality, manifestations that are an inherent component of the anomaly should not be coded separately. Additional codes should be assigned for manifestations that are not an inherent component. Codes from Chapter 17 may be used throughout the life of the patient. If a congenital malformation or deformity has been corrected, a personal history code should be used to identify the history of the malformation or deformity. Although present at birth, a malformation/deformation/or chromosomal abnormality may not be identified until later in life. Whenever the condition is diagnosed by the provider, it is appropriate to assign a code from codes Q00-QA1. For the birth admission, the appropriate code from category Z38, Liveborn infants, according to place of birth and type of delivery, should be sequenced as the principal diagnosis, followed by any congenital anomaly codes, Q00- QA1.
Index entries leading here3
Alongside this code6same parent — Q80
Medications1
MED-RT files conditions by MeSH, which carves the world differently from ICD-10. These are name matches on this code's description, offered as candidates — not as an assertion that they are this code.
Additional references
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.