The ICD-10-CM classifies CKD based on severity. The severity of CKD is designated by stages 1-5. Stage 2, code N18.2, equates to mild CKD; stage 3, codes N18.30-N18.32, equate to moderate CKD; and stage 4, code N18.4, equates to severe CKD. Code N18.6, End stage renal disease (ESRD), is assigned when the provider has documented end- stage renal disease (ESRD). If both a stage of CKD and ESRD are documented, assign code N18.6 only.
N49.3
BookmarkFournier gangrene
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
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- 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".
Exclusions10never code together
- certain conditions originating in the perinatal period (P04-P96)P04-P96
- certain infectious and parasitic diseases (A00-B99)A00-B99
- complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)Q00-Q99
- endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
- injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
- neoplasms (C00-D49)C00-D49
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94
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.
Official Guidelines3
ICD-10-CM Official Guidelines for Coding and Reporting, quoted in full. Published by CMS and NCHS; in the public domain.
Patients who have undergone kidney transplant may still have some form of chronic kidney disease (CKD) because the kidney transplant may not fully restore kidney function. Therefore, the presence of CKD alone does not constitute a transplant complication. Assign the appropriate N18 code for the patient’s stage of CKD and code Z94.0, Kidney transplant status. If a transplant complication such as failure or rejection or other transplant complication is documented, see section I.C.19.g for information on coding complications of a kidney transplant. If the documentation is unclear as to whether the patient has a complication of the transplant, query the provider.
Patients with CKD may also suffer from other serious conditions, most commonly diabetes mellitus and hypertension. The sequencing of the CKD code in relationship to codes for other contributing conditions is based on the conventions in the Tabular List. See I.C.9. Hypertensive chronic kidney disease. See I.C.19. Chronic kidney disease and kidney transplant complications.
Index entries leading here3
Alongside this code5same parent — N49
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.