MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Von Hippel-Lindau disease

ORPHA:892Kr.
Autosomal dominant

Von Voss-Cherstvoy syndrome

ORPHA:3439Malf.
Autosomal recessive

Von Willebrand disease

ORPHA:903Kr.
Autosomal dominant, 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

Vulvar adenocarcinoma

ORPHA:494454His. subt.

Vulvar basal cell carcinoma

ORPHA:494451His. subt.

Vulvar carcinoma

ORPHA:494418Kr.

Vulvar intraepithelial neoplasia

ORPHA:137583Kr.
Not applicable

Vulvar squamous cell carcinoma

ORPHA:494448His. subt.

Vulvovaginal gingival syndrome

ORPHA:83453Kr.
Not applicable

W syndrome

ORPHA:2804Malf.
X-linked recessive

WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome

ORPHA:466943Malf.
Autosomal dominant, Not applicable, Unknown

WAGR syndrome

ORPHA:893Malf.
Autosomal dominant

WARS2-related combined oxidative phosphorylation defect

ORPHA:572798Kr.
Autosomal recessive

WHIM syndrome

ORPHA:51636Kr.
Autosomal dominant, Autosomal recessive, Not applicable

WT limb-blood syndrome

ORPHA:3466Kr.
Autosomal dominant

Waardenburg syndrome

ORPHA:3440Kr.
Autosomal dominant, Autosomal recessive

Waardenburg syndrome type 1

ORPHA:894Kl. subt.
Autosomal dominant