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"

9 matching diseasesClear search ×

Dentin dysplasia type I

DD-I · DTDP1

ORPHA:99789

Dentin dysplasia

DD

ORPHA:1653

Dentin dysplasia type II

DD-II · DTDP2

ORPHA:99791

Fibromuscular dysplasia

FMD

ORPHA:698012

Oculodentodigital dysplasia

Oculo-dento-digital dysplasia · ODOD syndrome

ORPHA:2710

Otodental syndrome

Globodontia · Otodental dysplasia

ORPHA:2791

Otomandibular dysplasia

ORPHA:155896

Pelviscapular dysplasia

Cousin syndrome · Familial pelvis-scapular dysplasia

ORPHA:93333

Renal dysplasia

Kidney dysplasia

ORPHA:93108