MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Benign recurrent intrahepatic cholestasis type 1

ORPHA:99960Kl. subt.
Autosomal recessive

Benign recurrent intrahepatic cholestasis type 2

ORPHA:99961Kl. subt.
Autosomal recessive

Benign schwannoma

ORPHA:252164Kr.
Not applicable

Bernard-Soulier syndrome

ORPHA:274Kr.
Autosomal dominant, Autosomal recessive

Best vitelliform macular dystrophy

ORPHA:1243Kr.
Autosomal dominant

Beta-ketothiolase deficiency

ORPHA:134Kr.
Autosomal recessive

Beta-mannosidosis

ORPHA:118Kr.
Autosomal recessive

Beta-mercaptolactate cysteine disulfiduria

ORPHA:1035Bio-An.

Beta-propeller protein-associated neurodegeneration

ORPHA:329284Kr.
X-linked dominant

Beta-sarcoglycan-related limb-girdle muscular dystrophy R4

ORPHA:119Kr.
Autosomal recessive

Beta-thalassemia

ORPHA:848Kl. gruppe
Autosomal dominant, Autosomal recessive

Beta-thalassemia associated with another hemoglobin anomaly

ORPHA:231230Kat.
Autosomal dominant, Autosomal recessive

Beta-thalassemia intermedia

ORPHA:231222Kr.
Autosomal recessive

Beta-thalassemia major

ORPHA:231214Kr.
Autosomal recessive

Beta-thalassemia-X-linked thrombocytopenia syndrome

ORPHA:231393Kr.
X-linked recessive

Beta-ureidopropionase deficiency

ORPHA:65287Kr.
Autosomal recessive

Bethlem muscular dystrophy

ORPHA:610Kr.
Autosomal dominant, Autosomal recessive

Bickerstaff brainstem encephalitis

ORPHA:79138Kr.
Not applicable

Biemond syndrome type 2

ORPHA:141333Kr.
Unknown

Bietti crystalline dystrophy

ORPHA:41751Kr.
Autosomal recessive

Bifid nose

ORPHA:2695Malf.
Autosomal dominant, Autosomal recessive

Bifid uvula

ORPHA:99771Morph.
Multigenic/multifactorial, Not applicable

Bifunctional enzyme deficiency

ORPHA:300Kr.
Autosomal recessive

Bilateral acute depigmentation of the iris

ORPHA:69736Kr.
Unknown