MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Robinow syndrome

ORPHA:97360Malf.
Autosomal dominant, Autosomal recessive

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

Rothmund-Thomson syndrome type 1

ORPHA:221008Kl. subt.
Autosomal recessive

Rothmund-Thomson syndrome type 2

ORPHA:221016Kl. subt.
Autosomal recessive

Rothmund-Thomson syndrome type 3

ORPHA:715640Kl. subt.
Autosomal recessive

Rothmund-Thomson syndrome type 4

ORPHA:715635Kl. subt.
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

Rubinstein-Taybi syndrome

ORPHA:783Malf.
Autosomal dominant, Unknown

Rubinstein-Taybi syndrome due to 16p13.3 microdeletion

ORPHA:353281Ätl. subt.
Not applicable

Rubinstein-Taybi syndrome due to CREBBP mutations

ORPHA:353277Ätl. subt.
Autosomal dominant

Rubinstein-Taybi syndrome due to EP300 haploinsufficiency

ORPHA:353284Ätl. subt.
Autosomal dominant

Ruvalcaba syndrome

ORPHA:3121Malf.
Unknown

S-adenosylhomocysteine hydrolase deficiency

ORPHA:88618Kr.
Autosomal recessive