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"

16 matching diseasesClear search ×

Atelosteogenesis type II

Atelosteogenesis type 2 · De la Chapelle dysplasia

ORPHA:56304

Dentin dysplasia type I

DD-I · DTDP1

ORPHA:99789

Florid cemento-osseous dysplasia

Florid osseous dysplasia · Focal cemento-osseous dysplasia

ORPHA:83451

Focal facial dermal dysplasia type I

Bitemporal aplasia cutis congenita · Brauer syndrome

ORPHA:79133

Frontonasal dysplasia-alopecia-genital anomalies syndrome

ALX4-related FNDAG · Craniofrontonasal dysplasia with alopecia and hypogonadism

ORPHA:228390

Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome

ALX1-related frontonasal dysplasia · Frontonasal dysplasia type 3

ORPHA:306542

Frontorhiny

Frontonasal dysplasia type 1 · ALX3-related frontonasal dysplasia

ORPHA:391474

Heart-hand syndrome type 2

Atriodigital dysplasia type 2 · Tabatznik syndrome

ORPHA:1350

Heart-hand syndrome type 3

Atriodigital dysplasia type 3 · Cardiomelic syndrome type 3

ORPHA:1342

Holt-Oram syndrome

Atriodigital dysplasia type 1 · HOS

ORPHA:392

Immuno-osseous dysplasia

ORPHA:169349

Multiple epiphyseal dysplasia type 1

EDM1 · MED1

ORPHA:93308

Neonatal osteosclerotic dysplasia

ORPHA:93443

Oculodentodigital dysplasia

Oculo-dento-digital dysplasia · ODOD syndrome

ORPHA:2710

Schimke immuno-osseous dysplasia

Schimke syndrome · Spondyloepiphyseal dysplasia-nephrotic syndrome

ORPHA:1830

Thanatophoric dysplasia type 1

TD1 · Thanatophoric dwarfism type 1

ORPHA:1860