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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

RELA fusion-positive ependymoma

ORPHA:530792Ауру

REN-related autosomal dominant tubulointerstitial kidney disease

ORPHA:217330Клин. под.
Autosomal dominant

RERE-related neurodevelopmental syndrome

ORPHA:494344Мальф.
Autosomal dominant

RFT1-CDG

ORPHA:244310Ауру
Autosomal recessive

RFVT2-related riboflavin transporter deficiency

ORPHA:572543Клин. под.
Autosomal recessive

RFVT3-related riboflavin transporter deficiency

ORPHA:572550Клин. под.
Autosomal recessive

RHYNS syndrome

ORPHA:140976Ауру
Autosomal recessive

RIDDLE syndrome

ORPHA:420741Мальф.
Autosomal recessive

RIN2 syndrome

ORPHA:217335Мальф.
Autosomal recessive

RNASEH2B-related hereditary spastic paraplegia

ORPHA:689234Ауру
Autosomal recessive

RNF13-related severe early-onset epileptic encephalopathy

ORPHA:544503Ауру
Autosomal dominant

RNU4-2-related autosomal dominant neurodevelopmental disorder

ORPHA:686488Мальф.
Autosomal dominant

Rabies

ORPHA:770Ауру
Not applicable

Rabson-Mendenhall syndrome

ORPHA:769Мальф.
Autosomal recessive

Radial deficiency-tibial hypoplasia syndrome

ORPHA:1121Мальф.

Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome

ORPHA:2252Мальф.

Radial ray hypoplasia-choanal atresia syndrome

ORPHA:3026Мальф.
Autosomal dominant

Radiation proctitis

ORPHA:70475Ауру
Not applicable

Radio-renal syndrome

ORPHA:3015Мальф.

Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome

ORPHA:71289Мальф.
Autosomal dominant

Radioulnar synostosis-developmental delay-hypotonia syndrome

ORPHA:3270Мальф.
Unknown

Radioulnar synostosis-microcephaly-scoliosis syndrome

ORPHA:3268Мальф.
Unknown

Ramon syndrome

ORPHA:3019Мальф.
Autosomal recessive

Ramos-Arroyo syndrome

ORPHA:1051Мальф.
Autosomal dominant