Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
VACTERL/VATER association
Not applicable
Antenatal, Neonatal
VEXAS syndrome
Not applicable
Adult, Elderly
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 atresia
Not applicable
Childhood
Vaginal carcinoma
Adult, Elderly
Van den Ende-Gupta syndrome
Autosomal recessive
Infancy, Neonatal
Van der Woude syndrome
Autosomal dominant, Not applicable
Antenatal, Neonatal
Variably protease-sensitive prionopathy
Not applicable
Variant ABeta2M amyloidosis
Autosomal dominant
Adult
Variant Creutzfeldt-Jakob disease
Adult
Variant of Guillain-Barré syndrome
Multigenic/multifactorial, Not applicable
All ages
Variegate porphyria
Autosomal dominant
Adolescent, Adult
Vascular Ehlers-Danlos syndrome
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Vascular Ehlers-Danlos-polymicrogyria syndrome
Infancy, Neonatal
Vasculitis
Vegetative pyoderma gangrenosum
Multigenic/multifactorial
Adolescent, Adult, Childhood, Elderly
Vein of Galen malformation
Not applicable
Antenatal, Infancy, Neonatal
Velo-facial-skeletal syndrome
Neonatal
Venezuelan hemorrhagic fever
All ages
Ventilator-induced diaphragmatic dysfunction
All ages
Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome
Unknown
Infancy, Neonatal
Ventriculomegaly-cystic kidney disease
Autosomal recessive
Antenatal