MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Roch-Leri mesosomatous lipomatosis

ORPHA:529Kr.
Autosomal dominant

Rocky Mountain spotted fever

ORPHA:83311Kr.
Not applicable

Roifman syndrome

ORPHA:353298Kr.
Autosomal recessive

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

ORPHA:163727Kr.
Autosomal recessive

Rolandic epilepsy-speech dyspraxia syndrome

ORPHA:163721Kr.
Autosomal dominant, X-linked dominant

Romano-Ward syndrome

ORPHA:101016Kr.
Autosomal dominant, Autosomal recessive

Rombo syndrome

ORPHA:3110Kr.
Unknown

Rosaï-Dorfman disease

ORPHA:158014Kr.

Rothmund-Thomson syndrome

ORPHA:2909Kr.
Autosomal recessive

Rotor syndrome

ORPHA:3111Kr.
Autosomal recessive

Roussy-Lévy syndrome

ORPHA:3115Kr.
Autosomal dominant

Rowell syndrome

ORPHA:658584Kr.

Rubella panencephalitis

ORPHA:83616Kr.
Not applicable

S-adenosylhomocysteine hydrolase deficiency

ORPHA:88618Kr.
Autosomal recessive

SAMD9L-associated autoinflammatory syndrome

ORPHA:619367Kr.
Not applicable

SAPHO syndrome

ORPHA:793Kr.
Multigenic/multifactorial, Not applicable

SCALP syndrome

ORPHA:370052Kr.
Not applicable

SCGN-related severe early-onset hereditary ulcerative colitis

ORPHA:714481Kr.
Autosomal recessive

SHOX-related short stature

ORPHA:314795Kr.
Autosomal dominant

SIM1-related Prader-Willi-like syndrome

ORPHA:398079Kr.
Autosomal dominant

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

ORPHA:633014Kr.
Autosomal dominant, Autosomal recessive

SLC35A1-CDG

ORPHA:238459Kr.
No data available

SLC35A2-CDG

ORPHA:356961Kr.
Unknown

SLC39A8-CDG

ORPHA:468699Kr.
Autosomal recessive