Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Von Hippel-Lindau disease
Autosomal dominant
Adolescent, Adult, Childhood
Von Voss-Cherstvoy syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Von Willebrand disease
Autosomal dominant, Autosomal recessive
All ages
Von Willebrand disease type 1
Autosomal dominant
All ages
Von Willebrand disease type 2
Autosomal dominant, Autosomal recessive
All ages
Von Willebrand disease type 2A
Autosomal dominant, Autosomal recessive
Von Willebrand disease type 2B
Autosomal dominant
Von Willebrand disease type 2M
Autosomal dominant
Von Willebrand disease type 2N
Autosomal recessive
Von Willebrand disease type 3
Autosomal recessive
Infancy, Neonatal
Vulvar adenocarcinoma
Adult, Elderly
Vulvar basal cell carcinoma
Adult, Elderly
Vulvar carcinoma
Adult, Elderly
Vulvar intraepithelial neoplasia
Not applicable
Adult, Elderly
Vulvar squamous cell carcinoma
Adult, Elderly
Vulvovaginal gingival syndrome
Not applicable
Adult
W syndrome
X-linked recessive
Infancy, Neonatal
WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome
Autosomal dominant, Not applicable, Unknown
Childhood, Infancy
WAGR syndrome
Autosomal dominant
Antenatal, Neonatal
WARS2-related combined oxidative phosphorylation defect
Autosomal recessive
Infancy, Neonatal
WHIM syndrome
Autosomal dominant, Autosomal recessive, Not applicable
Adolescent, Adult, Childhood
WT limb-blood syndrome
Autosomal dominant
Childhood
Waardenburg syndrome
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Waardenburg syndrome type 1
Autosomal dominant
Neonatal