This is the American ICD-10-CM version of K82.0 - other international versions of ICD-10 K82.0 may differ. ICD-10-CM K83.8 is grouped within Diagnostic Related Group (s) (MS-DRG v40.0): 444 Disorders of the biliary tract with mcc 445 Disorders of the biliary tract with cc 446 Disorders of the biliary tract without cc/mcc Convert K83.8 to ICD-9-CM Code History 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM) Anomaly, cervix, in pregnancy or childbirth, Index Terms Starting With 'A' (Atresia, atretic), Absence (complete) (partial) of alimentary tract NOS, Malposition, congenital of digestive system, congenital stenosis of aortic valve in hypoplastic left heart syndrome (, supravalvular aortic stenosis (congenital) (, Obstruction of aqueduct of Sylvius, congenital, Congenital cerebral aneurysm (nonruptured), Congenital malformation of cerebral vessels NOS, Congenital atresia or stricture of osseous meatus, Atresia and stenosis of urethra and bladder neck NOS, Congenital obstruction of vesicourethral orifice, stricture and stenosis of cervix uteri complicating labor (, Obstructed labor due to conditions listed in, code to identify abnormality of pelvic organs, Congenital stenosis of nares (anterior) (posterior), Hypertrophy of cystic duct or gallbladder, Nonfunctioning of cystic duct or gallbladder, Occlusion of cystic duct or gallbladder without cholelithiasis, Stenosis of cystic duct or gallbladder without cholelithiasis, Stricture of cystic duct or gallbladder without cholelithiasis, obstruction of gallbladder with cholelithiasis (, Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS, Atresia of esophagus with broncho-esophageal fistula, Absence of fallopian tube and broad ligament, Accessory fallopian tube and broad ligament, Atresia of fallopian tube and broad ligament, Congenital malformation of fallopian tube or broad ligament NOS, Female infertility associated with congenital anomaly of tube, Female infertility due to tubal occlusion, Congenital malformation of gallbladder NOS, Congenital diverticulum of left ventricle, Congenital absence, atresia and stenosis of intestine NOS, code(s) to identify all associated manifestations, Congenital absence of salivary glands and ducts, Congenital accessory salivary glands and ducts, Benign lymphoepithelial lesion of salivary gland, Absence of vena cava (inferior) (superior), Azygos continuation of inferior vena cava, Partial anomalous pulmonary venous return, Total anomalous pulmonary venous return [TAPVR], subdiaphragmatic, Total anomalous pulmonary venous return [TAPVR], supradiaphragmatic. Request a Demo 14 Day Free Trial Buy Now Official Long Descriptor Obstruction of bile duct Occlusion of bile duct without cholelithiasis Sialolithiasis (also termed salivary calculi, or salivary stones) is a crystallopathy where a calcified mass or sialolith forms within a salivary gland, usually in the duct of the submandibular gland (also termed "Wharton's duct"). intraoperative cholangiogram (gallbladder and bile ducts with high osmolar contrast) H04.011 Acute dacryoadenitis, right lacrimal gland H04.012 Acute dacryoadenitis, left lacrimal gland intermittent hemodialysis performed for four hours, stenosis of dialysis arteriovenous fistula, initial encounter Request a Demo 14 Day Free Trial Buy Now Official Long Descriptor Neonatal obstruction of right nasolacrimal duct K82.0. percutaneous balloon angioplasty right radial artery, hypertensive end-stage renal disease, dialysis maintenance reh2021. Stenosis of cystic duct or gallbladder without mention of calculus Stricture of cystic duct or gallbladder without mention of calculus ICD-9-CM Volume 2 Index entries containing back-references to 575.2: Atresia, atretic (congenital) 759.89 cystic duct 751.61 acquired 575.8 with obstruction (see also Obstruction, gallbladder) 575.2 Constriction f(x)=lnx,0
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