Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome
Neonatal
White platelet syndrome
Autosomal dominant
No data available
White sponge nevus
Autosomal dominant
White-Sutton syndrome
Autosomal dominant
Antenatal, Infancy, Neonatal
Whooping cough
All ages
Wieacker-Wolff syndrome
Not applicable, X-linked recessive
Neonatal
Wiedemann-Rautenstrauch syndrome
Autosomal recessive
Antenatal, Neonatal
Wiedemann-Steiner syndrome
Autosomal dominant
Childhood, Infancy, Neonatal
Wild type ABeta2M amyloidosis
Not applicable
Adult
Wild type ATTR amyloidosis
Not applicable
Adult, Elderly
Wildervanck syndrome
Infancy, Neonatal
Williams syndrome
Autosomal dominant
Antenatal, Neonatal
Williams-Campbell syndrome
Not applicable
Adult, Childhood
Wilson disease
Autosomal recessive
Adolescent, Adult, Childhood, Elderly
Wilson-Turner syndrome
X-linked dominant, X-linked recessive
Childhood
Wiskott-Aldrich syndrome
Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive
Infancy, Neonatal
Witteveen-Kolk syndrome
Autosomal dominant
Antenatal, Neonatal
Wolcott-Rallison syndrome
Autosomal recessive
Infancy, Neonatal
Wolf-Hirschhorn syndrome
Multigenic/multifactorial, Not applicable
Antenatal, Neonatal
Wolfram syndrome
Autosomal recessive
Adolescent, Adult, Childhood
Wolfram-like syndrome
Autosomal dominant
Childhood
Wolman disease
Autosomal recessive
Infancy, Neonatal
Woodhouse-Sakati syndrome
Autosomal recessive
Adolescent, Childhood
Woolly hair
Autosomal dominant, Autosomal recessive
Infancy, Neonatal