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 ×

Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome

Skraban-Deardorff syndrome

ORPHA:513456

DEND syndrome

Developmental delay-epilepsy-neonatal diabetes syndrome

ORPHA:79134

Dent disease

Dent syndrome · Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis

ORPHA:1652

Diethylstilbestrol syndrome

DES embryofetopathy · DES syndrome

ORPHA:1916

Febrile infection-related epilepsy syndrome

AERRPS · Acute encephalitis with refractory repetitive partial seizures

ORPHA:163703

Fibular aplasia-complex brachydactyly syndrome

Du Pan syndrome

ORPHA:2639

Joubert syndrome with oculorenal defect

Arima syndrome · CORS

ORPHA:2318

Neuromyelitis optica spectrum disorder

Devic disease · Devic syndrome

ORPHA:71211

Neuromyelitis optica spectrum disorder with anti-AQP4 antibodies

Devic disease · Devic syndrome

ORPHA:592850

Neuromyelitis optica spectrum disorder with anti-MOG antibodies

Devic disease · Devic syndrome

ORPHA:592856

Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies

Devic disease · Devic syndrome

ORPHA:592869

Oculocerebrocutaneous syndrome

Delleman syndrome · Delleman-Oorthuys syndrome

ORPHA:1647

Zimmermann-Laband syndrome

Gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome · Laband syndrome

ORPHA:3473