Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
VIPoma
Not applicable
All ages
VPS11-related autosomal recessive hypomyelinating leukodystrophy
Autosomal recessive
Infancy
Vacuolar myopathy with sarcoplasmic reticulum protein aggregates
Autosomal dominant, Unknown
Adult
Vaginal carcinoma
Adult, Elderly
Variably protease-sensitive prionopathy
Not applicable
Variant ABeta2M amyloidosis
Autosomal dominant
Adult
Variant Creutzfeldt-Jakob disease
Adult
Variegate porphyria
Autosomal dominant
Adolescent, Adult
Vascular Ehlers-Danlos syndrome
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Vascular Ehlers-Danlos-polymicrogyria syndrome
Infancy, Neonatal
Venezuelan hemorrhagic fever
All ages
Ventriculomegaly-cystic kidney disease
Autosomal recessive
Antenatal
Vernal keratoconjunctivitis
Not applicable
Childhood
Verrucous hemangioma
Not applicable
Infancy, Neonatal
Very long chain acyl-CoA dehydrogenase deficiency
Autosomal recessive
Infancy, Neonatal
Vibratory urticaria
Autosomal dominant
All ages
Viral myositis
All ages
Virus-associated trichodysplasia spinulosa
Not applicable
All ages
Visual snow syndrome
Not applicable
Vitamin B12-responsive methylmalonic acidemia
Autosomal recessive
Childhood
Vitamin B12-unresponsive methylmalonic acidemia
Autosomal recessive
Childhood, Infancy, Neonatal
Vocal cord and pharyngeal distal myopathy
Autosomal dominant
Adult
Vogt-Koyanagi-Harada disease
Multigenic/multifactorial
All ages
Von Hippel-Lindau disease
Autosomal dominant
Adolescent, Adult, Childhood