MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

RELA fusion-positive ependymoma

ORPHA:530792Disease

REN-related autosomal dominant tubulointerstitial kidney disease

ORPHA:217330Clin. sub.
Autosomal dominant

RERE-related neurodevelopmental syndrome

ORPHA:494344Malform.
Autosomal dominant

RFT1-CDG

ORPHA:244310Disease
Autosomal recessive

RFVT2-related riboflavin transporter deficiency

ORPHA:572543Clin. sub.
Autosomal recessive

RFVT3-related riboflavin transporter deficiency

ORPHA:572550Clin. sub.
Autosomal recessive

RHYNS syndrome

ORPHA:140976Disease
Autosomal recessive

RIDDLE syndrome

ORPHA:420741Malform.
Autosomal recessive

RIN2 syndrome

ORPHA:217335Malform.
Autosomal recessive

RNASEH2B-related hereditary spastic paraplegia

ORPHA:689234Disease
Autosomal recessive

RNF13-related severe early-onset epileptic encephalopathy

ORPHA:544503Disease
Autosomal dominant

RNU4-2-related autosomal dominant neurodevelopmental disorder

ORPHA:686488Malform.
Autosomal dominant

Rabies

ORPHA:770Disease
Not applicable

Rabson-Mendenhall syndrome

ORPHA:769Malform.
Autosomal recessive

Radial deficiency-tibial hypoplasia syndrome

ORPHA:1121Malform.

Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome

ORPHA:2252Malform.

Radial ray hypoplasia-choanal atresia syndrome

ORPHA:3026Malform.
Autosomal dominant

Radiation proctitis

ORPHA:70475Disease
Not applicable

Radio-renal syndrome

ORPHA:3015Malform.

Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome

ORPHA:71289Malform.
Autosomal dominant

Radioulnar synostosis-developmental delay-hypotonia syndrome

ORPHA:3270Malform.
Unknown

Radioulnar synostosis-microcephaly-scoliosis syndrome

ORPHA:3268Malform.
Unknown

Ramon syndrome

ORPHA:3019Malform.
Autosomal recessive

Ramos-Arroyo syndrome

ORPHA:1051Malform.
Autosomal dominant