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 ×

Bencze syndrome

Hemifacial hyperplasia-strabismus syndrome

ORPHA:1241

Craniofacial dysostosis-diaphyseal hyperplasia syndrome

Autosomal dominant osteosclerosis, Stanescu type · Dysostosis, Stanescu type

ORPHA:1798

Hemifacial hyperplasia

Hemifacial hypertrophy

ORPHA:141145

Hemifacial myohyperplasia

ORPHA:141148

Hemihyperplasia-multiple lipomatosis syndrome

HHML

ORPHA:276280

Telecanthus-hypertelorism-strabismus-pes cavus syndrome

ORPHA:3293