National population-based cohort study of patients with newly diagnosed with HGD in England. The study used data collected prospectively as part of the National Oesophago-Gastric Cancer Audit (NOGCA). These records were linked to HES to investigate the pattern of ICD-10 codes recorded for these...
ICD-10: Q87.5 OMIM:248370608612 UMLS: C0432291 MeSH: - GARD:11893 下颌骨骨质疏松症基因解码、基因检测的不同名字 下颌骨骨质疏松症基因解码、基因检测mandibuloacral dysostosis gene decoding, gene test 下颌骨发育不良基因解码、基因检测Mandibuloacral dysplasia gene decoding,gene test ...
网络轻度阴道异常增生 网络释义 1. 轻度阴道异常增生 ICD 10 查询: N ... N890Mild vaginal dysplasia轻度阴道异常增生N891 Moderate vaginal dysplasia 中度阴道异常增生 ... icd-10th.blogspot.com|基于 1 个网页
DDH ICD-10Q65.9 Congenital deformity of hip, unspecified See all Congenital Hip ICD-10 codes. DDH ICD-9754 754.30 unilateral dislocation 754.31 bilateral dislocation 754.32 unilateral subluxation 754.33 bilateral subluxation 754.35 dislocation of one hip, subluxation of the other...
网络中度阴道异常增生 网络释义 1. 中度阴道异常增生 ICD 10 查询: N ... N890 Mild vaginal dysplasia 轻度阴道异常增生 N891Moderate vaginal dysplasia中度阴道异常增生... icd-10th.blogspot.com|基于 1 个网页
ICD-O-DA 7491.0 ICD-DA 526.85 Bone Tumor Key 325 Author information Authors and Affiliations Departement Chirurgie, Kantonsspital Basel, Universitätskliniken, Spitalstrasse 21, CH-4031, Basel, Switzerland PD Dr. med. et med. dent. Joachim Prein & Prof. Dr. med. et med. dent. Bernd Sp...
In order of priority, the algorithms searched for patient records that contained (1) specific ICD-10 codes for various ED disorders; (2) 2 or more cardinal ED features in different tissues (hypotrichosis, hypodontia, hypohidrosis, nail dystrophy); or (3) 1 cardinal ED feature ...
Objectives The purpose of this study was to define the incidence and predictors of implantable cardioverter-defibrillator (ICD) therapy in patients with ar... Aditya,Bhonsale,and,... - 《Journal of the American College of Cardiology》 被引量: 225发表: 2011年 Pitfalls in the diagnosis of arrh...
(FMD) in ∼10% of cases2. While atherosclerosis has been widely studied and its genetic architecture has been well defined, little is known about the pathogenesis or genetics of FMD. To date, onlyPHACTR1, a pleiotropic locus involved in the genetic risk of several cardiovascular and ...
In the univariate analysis, several clinical parameters including history of syncope, ICD, LV involvement on CMR, LVEF < 50%, presence of LGE, LV GRS <30.27%, GCS > −13.87%, GLS > −12.65% were univariate predictors of the cardiac endpoint. At first, we tested in multi...