Other names: ESSO
This ontology contains epilepsy syndromes, seizure types, and data elements associated with them.
The Epilepsy Ontology (EPO) is an assembly of structured knowledge on various aspects of epilepsy, developed according to basic formal ontology (BFO) and Open Biological and Biomedical Ontology (OBO) ...
The Epilepsy and Seizure Ontology (EpSO) is an application ontology developed to support epilepsy focused informatics tools for patient care and clinical research. EpSO is released by the Case Western ...
Ontology about the epilepsy domain and epileptic seizures. Based on the diagnosis proposed by the International League Against Epilepsy (ILAE).
Collection of samples and data across the following diseases: Epilepsy (disorder) The Epilepsy Society Brain and Tissue Bank is a recently established tissue bank at the Institute of Neurology, which ...
A prospective national clinical audit dataset which aims to include information on the investigation, diagnosis, treatment, care planning and outomes of all children and young people with a new onset ...
CarpeDB serves as a novel source for epilepsy researchers by featuring scores of "epilepsy genes" and associated publications in one locus. Furthermore, multiple genes implicated in epilepsy are also ...
An ontology designed to capture the semiology of epilepsy including ictal, post-ictal, inter-ictal, and aura signs. For the branches entitled "disease", "etiologic factor", "epidemiologic factor"--s ...
A dataset comprising a yearly survey of Trusts' paediatric epilepsy services
Ontology of epilepsy treatment, particularly for childbearing-age women with epilepsy.
The Functional Epilepsy Nomenclature for Ion Channels (FENICS) is allowing the consistent evaluation of electrophysiology experiments on Ion Channels in the context of neurological disorders, in parti ...
The Mapping of Epilepsy Ontologies (MEPO) provides owl:sameAs relationships of similar concepts for the ontologies EpSO, ESSO, EPILONT, EPISEM, and FENICS. Two concepts are considered similar if they ...
A curated database of mutations and polymorphisms associated with Lafora Progressive Myoclonus Epilepsy. The Lafora progressive myoclonus epilepsy mutation and polymorphism database is a collection of ...
Collection of samples and data across the following diseases: Sjogren's syndrome (disorder) Peripheral blood samples (DNA, RNA, serum, PBMC) from patients with primary Sjogren's syndrome, with detaile ...
A core reference ontology built upon BFO about exercise medicine. This ontology contains the related terms for healthy people, people with chronic conditions and people living with diability to exerci ...
A deeply phenotyped dataset of 61,000 patients being investigated or treated for acute coronary syndrome. Longitudinal linked healthcare utilisation data. Serial physiology readings, lab analysis res ...
This ontology contains entities such as: datatype, datatype generator, datatype quality and others giving the possibility to represent arbitrary complex datatypes. This is an important fact for a gene ...
This ontology contains the information of the frequency of usage and the relative frequency of usage of Human Gene Codons, to be used to the operations by The Project Of HIV Ontology.
Semantic data model of the set of common data elements for rare disease registration. To make rare disease registry data Interoperable (the 'I' in FAIR). Version 2.0. License CC0. Here, we present a s ...
This is a cohort study in patients with carpal tunnel syndrome. It contains both cross sectional (pre-surgery) as well as longitudinal data from patients undergoing decompression surgery (pre and 6 mo ...
Development and implementation of common data elements for venous thromboembolism research. Data Standards for Clinical Research. The International Society on Thrombosis and Haemostasis' Common Data ...