MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
727 Erkrankungen gefunden (Kl. subt.) Zurücksetzen

Vestibular schwannoma

ORPHA:252175Kl. subt.

Vitamin B12-responsive methylmalonic acidemia type cblA

ORPHA:79310Kl. subt.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia type cblB

ORPHA:79311Kl. subt.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia, type cblDv2

ORPHA:308442Kl. subt.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut-

ORPHA:79312Kl. subt.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut0

ORPHA:289916Kl. subt.
Autosomal recessive

Von Willebrand disease type 1

ORPHA:166078Kl. subt.
Autosomal dominant

Von Willebrand disease type 2

ORPHA:166081Kl. subt.
Autosomal dominant, Autosomal recessive

Von Willebrand disease type 2A

ORPHA:166084Kl. subt.
Autosomal dominant, Autosomal recessive

Von Willebrand disease type 2B

ORPHA:166087Kl. subt.
Autosomal dominant

Von Willebrand disease type 2M

ORPHA:166090Kl. subt.
Autosomal dominant

Von Willebrand disease type 2N

ORPHA:166093Kl. subt.
Autosomal recessive

Von Willebrand disease type 3

ORPHA:166096Kl. subt.
Autosomal recessive

Waardenburg syndrome type 1

ORPHA:894Kl. subt.
Autosomal dominant

Waardenburg syndrome type 2

ORPHA:895Kl. subt.
Autosomal dominant

Waardenburg syndrome type 3

ORPHA:896Kl. subt.
Autosomal dominant, Autosomal recessive

Wolman disease

ORPHA:75233Kl. subt.
Autosomal recessive

Wrinkly skin syndrome

ORPHA:2834Kl. subt.
Autosomal recessive

X-linked Alport syndrome

ORPHA:88917Kl. subt.
X-linked dominant

X-linked Alport syndrome-diffuse leiomyomatosis

ORPHA:1018Kl. subt.
X-linked dominant

X-linked agammaglobulinemia

ORPHA:47Kl. subt.
X-linked recessive

X-linked cerebral adrenoleukodystrophy

ORPHA:139396Kl. subt.
X-linked recessive

X-linked complicated corpus callosum dysgenesis

ORPHA:1497Kl. subt.
X-linked recessive

X-linked complicated spastic paraplegia type 1

ORPHA:306617Kl. subt.
X-linked recessive