Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Brain arteriovenous malformation
No data available
All ages
Brain dopamine-serotonin vesicular transport disease
Autosomal recessive
Infancy, Neonatal
Brain malformation-congenital heart disease-postaxial polydactyly syndrome
Unknown
Infancy, Neonatal
Brain-lung-thyroid syndrome
Autosomal dominant
Infancy, Neonatal
Branchio-oculo-facial syndrome
Autosomal dominant
Antenatal, Neonatal
Branchiogenic deafness syndrome
Autosomal dominant
Antenatal, Neonatal
Branchiootic syndrome
Autosomal dominant
Neonatal
Branchioskeletogenital syndrome
Autosomal recessive, X-linked dominant
Neonatal
Brazilian hemorrhagic fever
All ages
Breast implant-associated anaplastic large cell lymphoma
Not applicable
Adult, Elderly
Brittle cornea syndrome
Autosomal recessive
Infancy, Neonatal
Brody myopathy
Autosomal dominant, Autosomal recessive
Adolescent, Adult, Childhood
Bronchial neuroendocrine tumor
Not applicable
Adolescent, Adult, Childhood, Elderly
Bronchiolitis obliterans
Not applicable
All ages
Bronchogenic cyst
Unknown
All ages
Bronchopulmonary dysplasia
Not applicable
Infancy, Neonatal
Brooke-Spiegler syndrome
Autosomal dominant
Adolescent, Adult
Brucellosis
Not applicable
All ages
Bruck syndrome
Autosomal recessive
Antenatal, Childhood, Infancy, Neonatal
Brugada syndrome
Autosomal dominant, Not applicable
Adult, Childhood
Budd-Chiari syndrome
Multigenic/multifactorial
All ages
Buerger disease
Not applicable
Adult
Bullous diffuse cutaneous mastocytosis
Not applicable
Infancy, Neonatal
Bullous impetigo
Not applicable
All ages