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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 1,772 заболеваний (Мальф.) Қалпына келтіру

Retinal degeneration-nanophthalmos-glaucoma syndrome

ORPHA:1574Мальф.
Autosomal recessive

Retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome

ORPHA:3018Мальф.
Unknown

Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome

ORPHA:494439Мальф.
Autosomal recessive

Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome

ORPHA:3085Мальф.
Autosomal recessive

Revesz syndrome

ORPHA:3088Мальф.
Autosomal dominant

Rhizomelic dysplasia, Patterson-Lowry type

ORPHA:2831Мальф.

Rhizomelic syndrome, Urbach type

ORPHA:3098Мальф.

Rhombencephalosynapsis

ORPHA:59315Мальф.
Not applicable

Riboflavin transporter deficiency

ORPHA:97229Мальф.
Autosomal recessive

Richards-Rundle syndrome

ORPHA:1399Мальф.
Autosomal recessive

Richieri Costa-Pereira syndrome

ORPHA:3102Мальф.
Autosomal recessive

Richieri Costa-da Silva syndrome

ORPHA:3101Мальф.

Right isomerism

ORPHA:97548Мальф.
Autosomal recessive

Ring chromosome 1 syndrome

ORPHA:1437Мальф.

Ring chromosome 10 syndrome

ORPHA:1438Мальф.
Not applicable, Unknown

Ring chromosome 11 syndrome

ORPHA:96175Мальф.

Ring chromosome 12 syndrome

ORPHA:1439Мальф.

Ring chromosome 13 syndrome

ORPHA:96176Мальф.

Ring chromosome 14 syndrome

ORPHA:1440Мальф.
Not applicable, Unknown

Ring chromosome 15 syndrome

ORPHA:96177Мальф.

Ring chromosome 16 syndrome

ORPHA:96178Мальф.

Ring chromosome 17 syndrome

ORPHA:1441Мальф.
Not applicable, Unknown

Ring chromosome 18 syndrome

ORPHA:1442Мальф.

Ring chromosome 19 syndrome

ORPHA:1443Мальф.