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

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 carcinoma

ORPHA:180247Disease

Variably protease-sensitive prionopathy

ORPHA:454742Disease
Not applicable

Variant ABeta2M amyloidosis

ORPHA:314652Disease
Autosomal dominant

Variant Creutzfeldt-Jakob disease

ORPHA:576370Disease

Variegate porphyria

ORPHA:79473Disease
Autosomal dominant

Vascular Ehlers-Danlos syndrome

ORPHA:286Disease
Autosomal dominant, Autosomal recessive

Vascular Ehlers-Danlos-polymicrogyria syndrome

ORPHA:636941Disease

Venezuelan hemorrhagic fever

ORPHA:319234Disease

Ventriculomegaly-cystic kidney disease

ORPHA:443988Disease
Autosomal recessive

Vernal keratoconjunctivitis

ORPHA:70476Disease
Not applicable

Verrucous hemangioma

ORPHA:464318Disease
Not applicable

Very long chain acyl-CoA dehydrogenase deficiency

ORPHA:26793Disease
Autosomal recessive

Vibratory urticaria

ORPHA:493342Disease
Autosomal dominant

Viral myositis

ORPHA:206991Disease

Virus-associated trichodysplasia spinulosa

ORPHA:228379Disease
Not applicable

Visual snow syndrome

ORPHA:420556Disease
Not applicable

Vitamin B12-responsive methylmalonic acidemia

ORPHA:28Disease
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia

ORPHA:27Disease
Autosomal recessive

Vocal cord and pharyngeal distal myopathy

ORPHA:600Disease
Autosomal dominant

Vogt-Koyanagi-Harada disease

ORPHA:3437Disease
Multigenic/multifactorial

Von Hippel-Lindau disease

ORPHA:892Disease
Autosomal dominant