Search for a gene
IL7R - interleukin 7 receptor
Diseases list
- Disease-causing germline mutation(s) in Omenn syndrome
ORPHA:39041 - Disease-causing germline mutation(s) in T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
ORPHA:169154

Additional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources.