MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

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

Bifunctional enzyme deficiency

ORPHA:300Kr.
Autosomal recessive

Bilateral acute depigmentation of the iris

ORPHA:69736Kr.
Unknown

Bilateral striopallidodentate calcinosis

ORPHA:1980Kr.
Autosomal dominant, Autosomal recessive, Not applicable

Bile acid CoA ligase deficiency and defective amidation

ORPHA:276066Kr.
Unknown

Biliary cystadenocarcinoma

ORPHA:424982Kr.
Not applicable

Biotin-thiamine-responsive basal ganglia disease

ORPHA:65284Kr.
Autosomal recessive

Biotinidase deficiency

ORPHA:79241Kr.
Autosomal recessive

Birdshot chorioretinopathy

ORPHA:179Kr.
Unknown

Birk-Barel syndrome

ORPHA:166108Kr.
Autosomal dominant

Björnstad syndrome

ORPHA:123Kr.
Autosomal dominant, Autosomal recessive

Blastic plasmacytoid dendritic cell neoplasm

ORPHA:86870Kr.
Not applicable

Blau syndrome

ORPHA:90340Kr.
Autosomal dominant, Not applicable

Bleeding diathesis due to a collagen receptor defect

ORPHA:73271Kr.
Autosomal dominant, Autosomal recessive

Bleeding diathesis due to thromboxane synthesis deficiency

ORPHA:220443Kr.

Bleeding disorder due to CalDAG-GEFI deficiency

ORPHA:420566Kr.
Autosomal recessive

Bleeding disorder due to P2Y12 defect

ORPHA:36355Kr.
Autosomal recessive

Blepharoptosis-myopia-ectopia lentis syndrome

ORPHA:1259Kr.
Autosomal dominant

Blepharospasm-oromandibular dystonia syndrome

ORPHA:93964Kr.

Bloom syndrome

ORPHA:125Kr.
Autosomal recessive