MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

RELA fusion-positive ependymoma

ORPHA:530792Kr.

REN-related autosomal dominant tubulointerstitial kidney disease

ORPHA:217330Kl. subt.
Autosomal dominant

RERE-related neurodevelopmental syndrome

ORPHA:494344Malf.
Autosomal dominant

RFT1-CDG

ORPHA:244310Kr.
Autosomal recessive

RFVT2-related riboflavin transporter deficiency

ORPHA:572543Kl. subt.
Autosomal recessive

RFVT3-related riboflavin transporter deficiency

ORPHA:572550Kl. subt.
Autosomal recessive

RHYNS syndrome

ORPHA:140976Kr.
Autosomal recessive

RIDDLE syndrome

ORPHA:420741Malf.
Autosomal recessive

RIN2 syndrome

ORPHA:217335Malf.
Autosomal recessive

RNASEH2B-related hereditary spastic paraplegia

ORPHA:689234Kr.
Autosomal recessive

RNF13-related severe early-onset epileptic encephalopathy

ORPHA:544503Kr.
Autosomal dominant

RNU4-2-related autosomal dominant neurodevelopmental disorder

ORPHA:686488Malf.
Autosomal dominant

Rabies

ORPHA:770Kr.
Not applicable

Rabson-Mendenhall syndrome

ORPHA:769Malf.
Autosomal recessive

Radial deficiency-tibial hypoplasia syndrome

ORPHA:1121Malf.

Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome

ORPHA:2252Malf.

Radial ray hypoplasia-choanal atresia syndrome

ORPHA:3026Malf.
Autosomal dominant

Radiation proctitis

ORPHA:70475Kr.
Not applicable

Radio-renal syndrome

ORPHA:3015Malf.

Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome

ORPHA:71289Malf.
Autosomal dominant

Radioulnar synostosis-developmental delay-hypotonia syndrome

ORPHA:3270Malf.
Unknown

Radioulnar synostosis-microcephaly-scoliosis syndrome

ORPHA:3268Malf.
Unknown

Ramon syndrome

ORPHA:3019Malf.
Autosomal recessive

Ramos-Arroyo syndrome

ORPHA:1051Malf.
Autosomal dominant