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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 1,772 заболеваний (Порок) Сброс

Retinal degeneration-nanophthalmos-glaucoma syndrome

ORPHA:1574Порок
Autosomal recessive

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

ORPHA:3018Порок
Unknown

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

ORPHA:494439Порок
Autosomal recessive

Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome

ORPHA:3085Порок
Autosomal recessive

Revesz syndrome

ORPHA:3088Порок
Autosomal dominant

Rhizomelic dysplasia, Patterson-Lowry type

ORPHA:2831Порок

Rhizomelic syndrome, Urbach type

ORPHA:3098Порок

Rhombencephalosynapsis

ORPHA:59315Порок
Not applicable

Riboflavin transporter deficiency

ORPHA:97229Порок
Autosomal recessive

Richards-Rundle syndrome

ORPHA:1399Порок
Autosomal recessive

Richieri Costa-Pereira syndrome

ORPHA:3102Порок
Autosomal recessive

Richieri Costa-da Silva syndrome

ORPHA:3101Порок

Right isomerism

ORPHA:97548Порок
Autosomal recessive

Ring chromosome 1 syndrome

ORPHA:1437Порок

Ring chromosome 10 syndrome

ORPHA:1438Порок
Not applicable, Unknown

Ring chromosome 11 syndrome

ORPHA:96175Порок

Ring chromosome 12 syndrome

ORPHA:1439Порок

Ring chromosome 13 syndrome

ORPHA:96176Порок

Ring chromosome 14 syndrome

ORPHA:1440Порок
Not applicable, Unknown

Ring chromosome 15 syndrome

ORPHA:96177Порок

Ring chromosome 16 syndrome

ORPHA:96178Порок

Ring chromosome 17 syndrome

ORPHA:1441Порок
Not applicable, Unknown

Ring chromosome 18 syndrome

ORPHA:1442Порок

Ring chromosome 19 syndrome

ORPHA:1443Порок