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7 Patents Filed · HIPAA-Aligned · Free for Patients · Westwood, MA
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"
ATP6AP1-CDG
ATP6AP1-congenital disorder of glycosylation · ATPase H+ transporting accessory protein 1-congenital disorder of glycosylation
Autosomal non-syndromic agammaglobulinemia
Non-syndromic agammaglobulinemia, non-Bruton type · Non-syndromic hypogammaglobulinemia
Non-syndromic agammaglobulinemia
Non-syndromic hypogammaglobulinemia
Osteopetrosis-hypogammaglobulinemia syndrome
Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia · Autosomal recessive osteopetrosis type 7
Thymoma-hypogammaglobulinemia syndrome
Good syndrome
WHIM syndrome
WILM · Warts-hypogammaglobulinemia-infections-myelokathexis syndrome