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

Drug reaction with eosinophilia and systemic symptoms

ORPHA:139402Kr.
Not applicable

Drug-induced autoimmune hemolytic anemia

ORPHA:90037Kr.
Multigenic/multifactorial

Drug-induced localized lipodystrophy

ORPHA:90157Kr.

Drug-induced lupus erythematosus

ORPHA:231111Kr.
Not applicable

Dubin-Johnson syndrome

ORPHA:234Kr.
Autosomal recessive

Duchenne muscular dystrophy

ORPHA:98896Kr.
X-linked recessive

Dyggve-Melchior-Clausen disease

ORPHA:239Kr.
Autosomal recessive

Dysbetalipoproteinemia

ORPHA:412Kr.
Autosomal dominant, Multigenic/multifactorial

Dyschromatosis symmetrica hereditaria

ORPHA:41Kr.
Autosomal dominant

Dyschromatosis universalis hereditaria

ORPHA:241Kr.
Autosomal dominant, Autosomal recessive

Dysembryoplastic neuroepithelial tumor

ORPHA:251946Kr.
Not applicable

Dysequilibrium syndrome

ORPHA:1766Kr.
Autosomal recessive

Dysferlin-related limb-girdle muscular dystrophy R2

ORPHA:268Kr.
Autosomal recessive

Dyskeratosis congenita

ORPHA:1775Kr.
Autosomal dominant, Autosomal recessive, X-linked recessive

Dysplasia of head of femur, Meyer type

ORPHA:168621Kr.

Dyssegmental dysplasia, Rolland-Desbuquois type

ORPHA:156731Kr.

Dyssegmental dysplasia, Silverman-Handmaker type

ORPHA:1865Kr.
Autosomal recessive

Dystonia 16

ORPHA:210571Kr.
Autosomal recessive

Dystonia 28

ORPHA:589618Kr.
Autosomal dominant

Dystonia-aphonia syndrome

ORPHA:412217Kr.
Autosomal dominant

Dystonia-parkinsonism-hypermanganesemia syndrome

ORPHA:521406Kr.
Autosomal recessive

Dystrophic epidermolysis bullosa pruriginosa

ORPHA:89843Kr.
Autosomal dominant, Autosomal recessive

EAST syndrome

ORPHA:199343Kr.
Autosomal recessive

EBV-induced lymphoproliferative disease due to CARMIL2 deficiency

ORPHA:542301Kr.
Autosomal recessive