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"

8 matching diseasesClear search ×

Isotretinoin syndrome

Isotretinoin embryopathy · Retinoic acid embryopathy

ORPHA:2305

Acitretin/etretinate embryopathy

Fetal acitretin/etretinate syndrome · Retinoid embryopathy

ORPHA:40366

Diabetic embryopathy

Diabetes-induced teratogenicity

ORPHA:1926

Fetal valproate spectrum disorder

Fetal valproic acid syndrome · Valproic acid embryopathy

ORPHA:1906

Methimazole embryofetopathy

Methimazole/carbimazole embryofetopathy · Methimazole/carbimazole embryopathy

ORPHA:1923

Mycophenolate mofetil embryopathy

MMF embryopathy

ORPHA:268249

Propylthiouracil embryofetopathy

PTU embryofetopathy · PTU embryopathy

ORPHA:485358

Toluene embryopathy

ORPHA:1920