Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Verloove Vanhorick-Brubakk syndrome
Neonatal
Vernal keratoconjunctivitis
Not applicable
Childhood
Verrucous hemangioma
Not applicable
Infancy, Neonatal
Very long chain acyl-CoA dehydrogenase deficiency
Autosomal recessive
Infancy, Neonatal
Vestibular schwannoma
Vibratory urticaria
Autosomal dominant
All ages
Vici syndrome
Autosomal recessive
Antenatal, Neonatal
Viral hemorrhagic fever
Not applicable
All ages
Viral myositis
All ages
Virus-associated trichodysplasia spinulosa
Not applicable
All ages
Visceral arteriovenous malformation
Not applicable
Visceral heterotaxy
Autosomal dominant, Autosomal recessive, X-linked recessive
Infancy, Neonatal
Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome
Autosomal recessive
Antenatal, Neonatal
Visual snow syndrome
Not applicable
Vitamin B12-responsive methylmalonic acidemia
Autosomal recessive
Childhood
Vitamin B12-responsive methylmalonic acidemia type cblA
Autosomal recessive
Childhood
Vitamin B12-responsive methylmalonic acidemia type cblB
Autosomal recessive
Childhood
Vitamin B12-responsive methylmalonic acidemia, type cblDv2
Autosomal recessive
Vitamin B12-unresponsive methylmalonic acidemia
Autosomal recessive
Childhood, Infancy, Neonatal
Vitamin B12-unresponsive methylmalonic acidemia type mut-
Autosomal recessive
Infancy, Neonatal
Vitamin B12-unresponsive methylmalonic acidemia type mut0
Autosomal recessive
Infancy, Neonatal
Vitamin K antagonist embryofetopathy
Not applicable
Antenatal, Neonatal
Vocal cord and pharyngeal distal myopathy
Autosomal dominant
Adult
Vogt-Koyanagi-Harada disease
Multigenic/multifactorial
All ages