MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Verloove Vanhorick-Brubakk syndrome

ORPHA:3429Malform.

Vernal keratoconjunctivitis

ORPHA:70476Disease
Not applicable

Verrucous hemangioma

ORPHA:464318Disease
Not applicable

Very long chain acyl-CoA dehydrogenase deficiency

ORPHA:26793Disease
Autosomal recessive

Vestibular schwannoma

ORPHA:252175Clin. sub.

Vibratory urticaria

ORPHA:493342Disease
Autosomal dominant

Vici syndrome

ORPHA:1493Malform.
Autosomal recessive

Viral hemorrhagic fever

ORPHA:341Cat.
Not applicable

Viral myositis

ORPHA:206991Disease

Virus-associated trichodysplasia spinulosa

ORPHA:228379Disease
Not applicable

Visceral arteriovenous malformation

ORPHA:693855Clin. grp.
Not applicable

Visceral heterotaxy

ORPHA:450Cat.
Autosomal dominant, Autosomal recessive, X-linked recessive

Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome

ORPHA:73246Malform.
Autosomal recessive

Visual snow syndrome

ORPHA:420556Disease
Not applicable

Vitamin B12-responsive methylmalonic acidemia

ORPHA:28Disease
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia type cblA

ORPHA:79310Clin. sub.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia type cblB

ORPHA:79311Clin. sub.
Autosomal recessive

Vitamin B12-responsive methylmalonic acidemia, type cblDv2

ORPHA:308442Clin. sub.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia

ORPHA:27Disease
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut-

ORPHA:79312Clin. sub.
Autosomal recessive

Vitamin B12-unresponsive methylmalonic acidemia type mut0

ORPHA:289916Clin. sub.
Autosomal recessive

Vitamin K antagonist embryofetopathy

ORPHA:1914Malform.
Not applicable

Vocal cord and pharyngeal distal myopathy

ORPHA:600Disease
Autosomal dominant

Vogt-Koyanagi-Harada disease

ORPHA:3437Disease
Multigenic/multifactorial