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"

6 matching diseasesClear search ×

Mosaic neurofibromatosis type 1

MNF1 · Mosaic NF1

ORPHA:634461

Mosaic Legius syndrome

Mosaic NF1-like syndrome · Mosaic neurofibromatosis 1-like syndrome

ORPHA:634511

Mosaic NF2-related schwannomatosis

Mosaic neurofibromatosis type 2 · Mosaic NF2

ORPHA:634475

Mosaic schwannomatosis

Mosaic SWN · MNF3

ORPHA:634492

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