| Dataset | DISEASES Text-mining Gene-Disease Assocation Evidence Scores |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A severe combined immunodeficiency that is the result of a mutation on Chromosome 6 RAG1 gene involving genetic rearrangement of both the T- and B-lymphocyte receptor genes. (Human Disease Ontology, DOID_0060011) |
| Similar Terms | |
| Downloads & Tools |
1 genes co-occuring with the disease recombinase activating gene 1 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| RAG1 | recombination activating gene 1 | 1.05597 |
