|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Severe combined immunodeficiency (SCID) due to DCLRE1C deficiency is a type of SCID (see this term) characterized by severe and recurrent infections, diarrhea, failure to thrive, and cell sensitivity to ionizing radiation. (Orphanet Rare Disease Ontology, Orphanet_275)|
|Downloads & Tools|
1 genes associated with the severe combined immunodeficiency, athabascan type phenotype from the curated OMIM Gene-Disease Associations dataset.
|DCLRE1C||DNA cross-link repair 1C|