Disease coding systems for arthrogryposis multiplex congenita-Reference-Cited by-同舟云学术

Disease coding systems for arthrogryposis multiplex congenita

Published:2019-06-24 Issue:3 Volume:181 Page:304-309
ISSN:1552-4868
Container-title:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
language:en
Short-container-title:Am J Med Genet

Author:

Bedard Tanya¹^ORCID,Lowry R. Brian¹²³⁴

Affiliation:

1. Alberta Congenital Anomalies Surveillance System, Clinical GeneticsAlberta Health Services Calgary Alberta Canada

2. Department of PediatricsUniversity of Calgary and Alberta Children's Hospital Calgary Alberta Canada

3. Department of Medical GeneticsUniversity of Calgary and Alberta Children's Hospital Calgary Alberta Canada

4. Alberta Children's Hospital Research Institute, University of Calgary Calgary Alberta Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.c.31718

Reference14 articles.

1. Rare diseases in ICD11: making rare diseases visible in health information systems through appropriate coding

2. International multidisciplinary collaboration toward an annotated definition of arthrogryposis multiplex congenita

3. AMC REGISTRY: Arthrogryposis multiplex congenita registry on epidemiology, etiology, genomics and interventions targeting research in youth: Findings from the pilot study;Dahan‐Oliel N.;American Journal of Medical Genetics. Part C, Seminars in Medical Genetics,2019

4. European Commission Expert Group on Rare Diseases. (2014). Recommendation on ways to improve codification for rare diseases in health information systems: Adopted at the 3rd meeting of the Commission Expert Group on Rare Diseases November 12–13 2014. Retrieved fromhttps://ec.europa.eu/health//sites/health/files/rare_diseases/docs/recommendation_coding_cegrd_en.pdf

5. The Human Phenotype Ontology in 2017

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1. The Human Phenotype Ontology in 2024: phenotypes around the world;Nucleic Acids Research;2023-11-11

2. Epidemiology, aetiology, interventions and genomics in children with arthrogryposis multiplex congenita: protocol for a multisite registry;BMJ Open;2022-10

3. A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita;Genes;2021-07-08

4. Collaborating to advance interdisciplinary care for individuals with arthrogryposis;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2019-08-31

5. Research platform for children with arthrogryposis multiplex congenita: Findings from the pilot registry;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2019-07-29