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"

8 matching diseasesClear search ×

Fleck corneal dystrophy

FCD · François-Neetens speckled corneal dystrophy

ORPHA:98970

Isolated focal cortical dysplasia type I

FCD type I

ORPHA:268961

Isolated focal cortical dysplasia type Ia

FCD type Ia

ORPHA:268973

Isolated focal cortical dysplasia type Ib

FCD type Ib

ORPHA:268980

Isolated focal cortical dysplasia type Ic

FCD type Ic

ORPHA:268987

Isolated focal cortical dysplasia type II

Cortical dysplasia, Taylor type · FCD type II

ORPHA:268994

Isolated focal cortical dysplasia type IIa

FCD type IIa

ORPHA:269001

Isolated focal cortical dysplasia type IIb

FCD type IIb

ORPHA:269008