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"

13 matching diseasesClear search ×

Brachydactyly type A6

Osebold-Remondini syndrome · Acromesomelic dysplasia, Osebold-Remondini type

ORPHA:93382

Acromelic dysplasia

ORPHA:93436

Acromesomelic dysplasia

ORPHA:93437

Acromesomelic dysplasia, Grebe type

Chondrodysplasia, Grebe type

ORPHA:2098

Acromesomelic dysplasia, Hunter-Thompson type

Acromesomelic dwarfism

ORPHA:968

Acromesomelic dysplasia, Maroteaux type

ORPHA:40

Mesomelic and rhizo-mesomelic dysplasia

ORPHA:93438

Mesomelic dwarfism-cleft palate-camptodactyly syndrome

Reardon-Hall-Slaney syndrome · Mesomelic dysplasia, Reardon type

ORPHA:2631

Mesomelic dysplasia, Kantaputra type

Kantaputra mesomelic dysplasia · MDK

ORPHA:1836

Mesomelic dysplasia, Nievergelt type

Nievergelt syndrome · Mesomelic dwarfism, Nievergelt type

ORPHA:2633

Mesomelic dysplasia, Savarirayan type

Mesomelic dysplasia with absent fibulas and triangular tibias · Triangular tibia-fibular aplasia syndrome

ORPHA:85170

OBSOLETE: Acromesomelic dysplasia, Brahimi-Bacha type

ORPHA:953

Upper limb mesomelic dysplasia, type Fryns

Fryns-Hofkens-Fabry syndrome

ORPHA:2497