Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Waardenburg syndrome type 2
Autosomal dominant
Neonatal
Waardenburg syndrome type 3
Autosomal dominant, Autosomal recessive
Neonatal
Waardenburg-Shah syndrome
Autosomal dominant, Autosomal recessive
Neonatal
Wagner disease
Autosomal dominant
Childhood
Waldenström macroglobulinemia
Multigenic/multifactorial
Elderly
Walker-Warburg syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Warsaw breakage syndrome
Autosomal recessive
Infancy, Neonatal
Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome
Infancy, Neonatal
Warty dyskeratoma
Unknown
Adult
Weaver syndrome
Autosomal dominant, Not applicable
Antenatal, Neonatal
Weaver-Williams syndrome
Autosomal recessive
Infancy, Neonatal
Weill-Marchesani syndrome
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Weismann-Netter syndrome
Neonatal
Weiss-Kruszka Syndrome
Autosomal dominant
Antenatal, Neonatal
Well-differentiated fetal adenocarcinoma of the lung
Not applicable
All ages
Well-differentiated liposarcoma
Not applicable
Adult
Well-differentiated thymic neuroendocrine carcinoma
Not applicable
Adult
Wells syndrome
Not applicable
Adult
Werner syndrome
Autosomal recessive
Adolescent, Adult
West-Nile encephalitis
Not applicable
All ages
Western equine encephalitis
Not applicable
All ages
Whipple disease
Not applicable
No data available
White fibrous papulosis of the neck
Not applicable
Adult
White forelock with malformations
Infancy, Neonatal