MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
1,772 diseases matched (Malform.) Reset

Retinal degeneration-nanophthalmos-glaucoma syndrome

ORPHA:1574Malform.
Autosomal recessive

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

ORPHA:3018Malform.
Unknown

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

ORPHA:494439Malform.
Autosomal recessive

Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome

ORPHA:3085Malform.
Autosomal recessive

Revesz syndrome

ORPHA:3088Malform.
Autosomal dominant

Rhizomelic dysplasia, Patterson-Lowry type

ORPHA:2831Malform.

Rhizomelic syndrome, Urbach type

ORPHA:3098Malform.

Rhombencephalosynapsis

ORPHA:59315Malform.
Not applicable

Riboflavin transporter deficiency

ORPHA:97229Malform.
Autosomal recessive

Richards-Rundle syndrome

ORPHA:1399Malform.
Autosomal recessive

Richieri Costa-Pereira syndrome

ORPHA:3102Malform.
Autosomal recessive

Richieri Costa-da Silva syndrome

ORPHA:3101Malform.

Right isomerism

ORPHA:97548Malform.
Autosomal recessive

Ring chromosome 1 syndrome

ORPHA:1437Malform.

Ring chromosome 10 syndrome

ORPHA:1438Malform.
Not applicable, Unknown

Ring chromosome 11 syndrome

ORPHA:96175Malform.

Ring chromosome 12 syndrome

ORPHA:1439Malform.

Ring chromosome 13 syndrome

ORPHA:96176Malform.

Ring chromosome 14 syndrome

ORPHA:1440Malform.
Not applicable, Unknown

Ring chromosome 15 syndrome

ORPHA:96177Malform.

Ring chromosome 16 syndrome

ORPHA:96178Malform.

Ring chromosome 17 syndrome

ORPHA:1441Malform.
Not applicable, Unknown

Ring chromosome 18 syndrome

ORPHA:1442Malform.

Ring chromosome 19 syndrome

ORPHA:1443Malform.