Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

3 matching diseasesClear search ×

OBSOLETE: Common variable immunodeficiency due to an intrinsic B cell defect

OBSOLETE: CVID due to an intrinsic B cell defect

ORPHA:77303

OBSOLETE: Common variable immunodeficiency due to an intrinsic T cell defect

OBSOLETE: CVID due to an intrinsic T cell defect

ORPHA:99831

OBSOLETE: Common variable immunodeficiency due to TNFR deficiency

OBSOLETE: CVID due to TNFR deficiency

ORPHA:183672