MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Roch-Leri mesosomatous lipomatosis

ORPHA:529Disease
Autosomal dominant

Rocky Mountain spotted fever

ORPHA:83311Disease
Not applicable

Roifman syndrome

ORPHA:353298Disease
Autosomal recessive

Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome

ORPHA:163727Disease
Autosomal recessive

Rolandic epilepsy-speech dyspraxia syndrome

ORPHA:163721Disease
Autosomal dominant, X-linked dominant

Romano-Ward syndrome

ORPHA:101016Disease
Autosomal dominant, Autosomal recessive

Rombo syndrome

ORPHA:3110Disease
Unknown

Rosaï-Dorfman disease

ORPHA:158014Disease

Rothmund-Thomson syndrome

ORPHA:2909Disease
Autosomal recessive

Rotor syndrome

ORPHA:3111Disease
Autosomal recessive

Roussy-Lévy syndrome

ORPHA:3115Disease
Autosomal dominant

Rowell syndrome

ORPHA:658584Disease

Rubella panencephalitis

ORPHA:83616Disease
Not applicable

S-adenosylhomocysteine hydrolase deficiency

ORPHA:88618Disease
Autosomal recessive

SAMD9L-associated autoinflammatory syndrome

ORPHA:619367Disease
Not applicable

SAPHO syndrome

ORPHA:793Disease
Multigenic/multifactorial, Not applicable

SCALP syndrome

ORPHA:370052Disease
Not applicable

SCGN-related severe early-onset hereditary ulcerative colitis

ORPHA:714481Disease
Autosomal recessive

SHOX-related short stature

ORPHA:314795Disease
Autosomal dominant

SIM1-related Prader-Willi-like syndrome

ORPHA:398079Disease
Autosomal dominant

SLC12A2-related developmental delay-intellectual disability-sensorineural deafness syndrome

ORPHA:633014Disease
Autosomal dominant, Autosomal recessive

SLC35A1-CDG

ORPHA:238459Disease
No data available

SLC35A2-CDG

ORPHA:356961Disease
Unknown

SLC39A8-CDG

ORPHA:468699Disease
Autosomal recessive