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"

4 matching diseasesClear search ×

Mosaic neurofibromatosis type 1

MNF1 · Mosaic NF1

ORPHA:634461

Neurofibromatosis type 1

neurofibromatosis type I · NF-1

ORPHA:ORPHA:636

Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion

NF-1 · NF1

ORPHA:363700

Glycogen storage disease due to glucose-6-phosphatase deficiency

G6P deficiency · GSD due to G6P deficiency

ORPHA:364