MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

VACTERL/VATER association

ORPHA:887Malform.
Not applicable

VEXAS syndrome

ORPHA:596753Disease
Not applicable

VIPoma

ORPHA:97282Disease
Not applicable

VPS11-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:466934Disease
Autosomal recessive

Vacuolar myopathy with sarcoplasmic reticulum protein aggregates

ORPHA:88635Disease
Autosomal dominant, Unknown

Vaginal atresia

ORPHA:65681Morph.
Not applicable

Vaginal carcinoma

ORPHA:180247Disease

Van den Ende-Gupta syndrome

ORPHA:2460Malform.
Autosomal recessive

Van der Woude syndrome

ORPHA:888Malform.
Autosomal dominant, Not applicable

Variably protease-sensitive prionopathy

ORPHA:454742Disease
Not applicable

Variant ABeta2M amyloidosis

ORPHA:314652Disease
Autosomal dominant

Variant Creutzfeldt-Jakob disease

ORPHA:576370Disease

Variant of Guillain-Barré syndrome

ORPHA:231413Cat.
Multigenic/multifactorial, Not applicable

Variegate porphyria

ORPHA:79473Disease
Autosomal dominant

Vascular Ehlers-Danlos syndrome

ORPHA:286Disease
Autosomal dominant, Autosomal recessive

Vascular Ehlers-Danlos-polymicrogyria syndrome

ORPHA:636941Disease

Vasculitis

ORPHA:52759Cat.

Vegetative pyoderma gangrenosum

ORPHA:538872Clin. sub.
Multigenic/multifactorial

Vein of Galen malformation

ORPHA:1053Morph.
Not applicable

Velo-facial-skeletal syndrome

ORPHA:3424Malform.

Venezuelan hemorrhagic fever

ORPHA:319234Disease

Ventilator-induced diaphragmatic dysfunction

ORPHA:505395Situation

Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome

ORPHA:3201Malform.
Unknown

Ventriculomegaly-cystic kidney disease

ORPHA:443988Disease
Autosomal recessive