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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Robinow syndrome

ORPHA:97360Malform.
Autosomal dominant, Autosomal recessive

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

Rothmund-Thomson syndrome type 1

ORPHA:221008Clin. sub.
Autosomal recessive

Rothmund-Thomson syndrome type 2

ORPHA:221016Clin. sub.
Autosomal recessive

Rothmund-Thomson syndrome type 3

ORPHA:715640Clin. sub.
Autosomal recessive

Rothmund-Thomson syndrome type 4

ORPHA:715635Clin. sub.
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

Rubinstein-Taybi syndrome

ORPHA:783Malform.
Autosomal dominant, Unknown

Rubinstein-Taybi syndrome due to 16p13.3 microdeletion

ORPHA:353281Etio. sub.
Not applicable

Rubinstein-Taybi syndrome due to CREBBP mutations

ORPHA:353277Etio. sub.
Autosomal dominant

Rubinstein-Taybi syndrome due to EP300 haploinsufficiency

ORPHA:353284Etio. sub.
Autosomal dominant

Ruvalcaba syndrome

ORPHA:3121Malform.
Unknown

S-adenosylhomocysteine hydrolase deficiency

ORPHA:88618Disease
Autosomal recessive