MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Von Willebrand disease

ORPHA:903Disease
Autosomal dominant, Autosomal recessive

Vulvar carcinoma

ORPHA:494418Disease

Vulvar intraepithelial neoplasia

ORPHA:137583Disease
Not applicable

Vulvovaginal gingival syndrome

ORPHA:83453Disease
Not applicable

WARS2-related combined oxidative phosphorylation defect

ORPHA:572798Disease
Autosomal recessive

WHIM syndrome

ORPHA:51636Disease
Autosomal dominant, Autosomal recessive, Not applicable

WT limb-blood syndrome

ORPHA:3466Disease
Autosomal dominant

Waardenburg syndrome

ORPHA:3440Disease
Autosomal dominant, Autosomal recessive

Waardenburg-Shah syndrome

ORPHA:897Disease
Autosomal dominant, Autosomal recessive

Wagner disease

ORPHA:898Disease
Autosomal dominant

Waldenström macroglobulinemia

ORPHA:33226Disease
Multigenic/multifactorial

Walker-Warburg syndrome

ORPHA:899Disease
Autosomal recessive

Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome

ORPHA:568056Disease

Warty dyskeratoma

ORPHA:69745Disease
Unknown

Well-differentiated fetal adenocarcinoma of the lung

ORPHA:284395Disease
Not applicable

Wells syndrome

ORPHA:901Disease
Not applicable

Werner syndrome

ORPHA:902Disease
Autosomal recessive

West-Nile encephalitis

ORPHA:83476Disease
Not applicable

Western equine encephalitis

ORPHA:83593Disease
Not applicable

Whipple disease

ORPHA:3452Disease
Not applicable

White fibrous papulosis of the neck

ORPHA:228290Disease
Not applicable

White platelet syndrome

ORPHA:370131Disease
Autosomal dominant

White sponge nevus

ORPHA:171723Disease
Autosomal dominant

White-Sutton syndrome

ORPHA:468678Disease
Autosomal dominant