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"

10 matching diseasesClear search ×

Osteonecrosis of genetic origin

Bone necrosis of genetic origin

ORPHA:399380

Avascular necrosis of genetic origin

ORPHA:399388

Dysostosis of genetic origin

ORPHA:404568

Genetic 46,XY difference of sex development of endocrine origin

Genetic 46,XY DSD of endocrine origin · Genetic 46,XY disorder of sex development of endocrine origin

ORPHA:325713

Genetic bone tumor

ORPHA:183527

Kienbock disease

Aseptic necrosis of the lunate bone · Lunatomalacia

ORPHA:97332

Osteochondrosis of genetic origin

ORPHA:399391

Osteochondrosis of the tarsal bone

Avascular necrosis of the tarsal bone · Kohler disease

ORPHA:563991

Osteonecrosis

Bone necrosis

ORPHA:399158

Renal tubular dysgenesis of genetic origin

ORPHA:97369