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"

5 matching diseasesClear search ×

Sheldon-Hall syndrome

SSH · DA2B

ORPHA:1147

Atypical Rett syndrome

Atypical RTT · Rett syndrome variant

ORPHA:3095

Blepharophimosis-intellectual disability syndrome, SBBYS type

SBBYS variant of Ohdo syndrome · Hypothyroidism-dysmorphism-postaxial polydactyly-intellectual disability syndrome

ORPHA:3047

Freeman-Sheldon syndrome

Craniocarpotarsal dysplasia · Craniocarpotarsal dystrophy

ORPHA:2053

Frey syndrome

Baillarger syndrome · Auriculotemporal syndrome

ORPHA:662240