orphanet-rare-diseases-issues / RD-CODELinks
In the framework of the RD-CODE project, Orphanet provides a set of files, the Orphanet nomenclature files for coding, intended to be used to implement the Orphanet nomenclature in Health Information Systems for codification purposes.
☆13Updated 9 months ago
Alternatives and similar repositories for RD-CODE
Users that are interested in RD-CODE are comparing it to the libraries listed below
Sorting:
- loinc2hpo Annotation Data☆24Updated 2 years ago
- Repository for the GA4GH phenopacket schema☆87Updated 8 months ago
- Perform text mining for identification of HPO terms in free text from scientific publication.☆12Updated 11 months ago
- The Unified Phenotype Ontology (uPheno) integrates multiple phenotype ontologies into a unified cross-species phenotype ontology.☆79Updated 2 weeks ago
- a web application to search and navigate the Human Phenotype Ontology (HPO)☆14Updated 2 weeks ago
- Java library to map LOINC-encoded test results to Human Phenotype Ontology☆31Updated last year
- Collections of GA4GH phenopackets that represent individuals with Mendelian diseases.☆24Updated last week
- Transforming SemRep Predications into an Open Biomedical Linked Data Resource☆11Updated 7 years ago
- The symptom ontology was designed around the guiding concept of a symptom being: “A perceived change in function, sensation or appearance…☆41Updated last year
- Public release of the DeepPhe analytic software☆30Updated 2 years ago
- Semantic data model of the set of common data elements for rare disease registration☆12Updated last year
- ☆41Updated 5 years ago
- PhenoTagger☆56Updated last year
- phenol: Phenotype ontology library☆23Updated last month
- Tool that converts between BioC XML files and BioC JSON files☆16Updated 8 years ago
- Medical action ontology☆56Updated this week
- A software toolkit for the interconversion of standard data models for phenotypic data☆14Updated 3 weeks ago
- Python Phenopacket Tools☆14Updated 4 months ago
- ☆26Updated 5 years ago
- A stitching platform for InXight☆15Updated 2 months ago
- An app and library for building, conversion, and validation of GA4GH Phenopackets.☆15Updated last month
- The Gene Ontology Helpdesk☆16Updated 4 months ago
- The Ontology for Biomedical Investigations☆82Updated last week
- A collaborative guidebook for reusable data best practices☆13Updated 2 years ago
- Ontology for representing scientific evidence and provenance information☆50Updated 10 months ago
- Phenotype and genotype-based patient similarity☆11Updated 5 years ago
- using AI model to infer patient phenotypes from identified named entities (instances of biomedical concepts)☆10Updated 2 years ago
- SNP Extraction Tool for Human Variations☆27Updated last year
- ☆10Updated last month
- Ontology Based Profile Matching☆17Updated 3 years ago