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 ×

Twin to twin transfusion syndrome

Feto-fetal transfusion syndrome

ORPHA:95431

Aminopterin/methotrexate embryofetopathy

Aminopterin embryopathy syndrome · Fetal aminopterin syndrome

ORPHA:1908

Cocaine embryofetopathy

Fetal cocaine syndrome

ORPHA:1911

Congenital rubella syndrome

Mother-to-child transmission of rubella syndrome · CRS

ORPHA:290

Fetal alcohol syndrome

ARBD · ARND

ORPHA:1915

Fetal encasement syndrome

ORPHA:465824

Fetal hydantoin syndrome

Fetal dihydantoin syndrome · Phenytoin embryofetopathy

ORPHA:1912

Fetal iodine syndrome

ORPHA:1910

Fetal minoxidil syndrome

Minoxidil antenatal exposure

ORPHA:1918

Fetal parvovirus syndrome

Mother-to-child transmission of parvovirus syndrome · Parvovirus antenatal infection

ORPHA:295

Fetal trimethadione syndrome

ORPHA:1913

Fetal valproate spectrum disorder

Fetal valproic acid syndrome · Valproic acid embryopathy

ORPHA:1906

Indomethacin embryofetopathy

Fetal indomethacin syndrome

ORPHA:1909

Robinow syndrome

Acral dysostosis with facial and genital abnormalities · Fetal face syndrome

ORPHA:97360

Thalidomide embryopathy

Fetal thalidomide syndrome

ORPHA:3312

Tumor necrosis factor receptor 1 associated periodic syndrome

Familial Hibernian fever · TNF receptor 1-associated periodic syndrome

ORPHA:32960