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 ×

Hemifacial hyperplasia

Hemifacial hypertrophy

ORPHA:141145

Familial juvenile hypertrophy of the breast

Familial juvenile gigantomastia · Virginal breast hypertrophy

ORPHA:180176

Hemifacial myohyperplasia

ORPHA:141148

Hemifacial spasm

Facial hemispasm · Focal myoclonus of face

ORPHA:221083

Isolated hemihyperplasia

Hemi 3 syndrome · Hemicorporal hypertrophy

ORPHA:2128

Lower limb hypertrophy

ORPHA:295051

Progressive hemifacial atrophy

Hemifacial atrophy · PHA

ORPHA:1214

Upper limb hypertrophy

ORPHA:295049