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 ×

EDICT syndrome

Autosomal dominant keratoconus with early-onset anterior polar cataracts · Endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome

ORPHA:293936

Congenital aphakia-iris hypoplasia-microphthalmia-microcornea syndrome

ORPHA:617449

Congenital hereditary endothelial dystrophy type I

Autosomal dominant CHED · Autosomal dominant congenital hereditary endothelial dystrophy

ORPHA:98975

Congenital hereditary endothelial dystrophy type II

Congenital hereditary endothelial dystrophy type 2 · Infantile hereditary endothelial dystrophy

ORPHA:293603

Congenital muscular dystrophy-cataract-intellectual disability syndrome

INPP5K-related syndrome

ORPHA:662184

Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome

Bassoe syndrome

ORPHA:1875

Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome

ORPHA:488197

Hypomyelination-congenital cataract syndrome

ORPHA:85163