MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Reflex epilepsy

ORPHA:310Kl. gruppe

Refractory anemia with excess blasts in transformation

ORPHA:168960Kr.

Refractory celiac disease

ORPHA:398063Kr.
Not applicable

Refractory cytopenia with multilineage dysplasia

ORPHA:86836Kl. gruppe

Regional odontodysplasia

ORPHA:83450Kr.
Not applicable

Regional variant of Guillain-Barré syndrome

ORPHA:231416Kl. gruppe
Multigenic/multifactorial, Not applicable

Regressive spondylometaphyseal dysplasia

ORPHA:448267Malf.
Autosomal recessive

Reis-Bücklers corneal dystrophy

ORPHA:98961Kr.
Autosomal dominant

Relapsing fever

ORPHA:91547Kr.
Not applicable

Relapsing polychondritis

ORPHA:728Kr.
Unknown

Renal agenesis

ORPHA:411709Morph.
Autosomal dominant, Autosomal recessive

Renal agenesis, bilateral

ORPHA:1848Kl. subt.
Autosomal recessive

Renal agenesis, unilateral

ORPHA:93100Kl. subt.
Autosomal dominant

Renal arteriovenous malformation

ORPHA:693839Malf.
Not applicable

Renal caliceal diverticuli-deafness syndrome

ORPHA:2838Malf.

Renal cell carcinoma

ORPHA:217071Kl. gruppe
Not applicable

Renal coloboma syndrome

ORPHA:1475Malf.
Autosomal dominant

Renal dysplasia

ORPHA:93108Morph.
Autosomal dominant, Not applicable

Renal dysplasia, bilateral

ORPHA:93173Kl. subt.
Autosomal dominant, Not applicable

Renal dysplasia, unilateral

ORPHA:93172Kl. subt.
Autosomal dominant, Not applicable

Renal hypoplasia

ORPHA:93101Morph.
Autosomal dominant, Not applicable

Renal hypoplasia, bilateral

ORPHA:97362Kl. subt.
Autosomal dominant, Not applicable

Renal hypoplasia, unilateral

ORPHA:97361Kl. subt.
Not applicable

Renal medullary carcinoma

ORPHA:319319Kr.