Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Spinal epidural arteriovenous malformation
Unknown
Split cord malformation type I
Adolescent, Adult, Childhood, Infancy
Split cord malformation type II
Adolescent, Adult, Childhood, Infancy
Split cord malformation, composite type
Sprengel deformity
Antenatal, Infancy, Neonatal
Sternal cleft
Not applicable
Antenatal, Neonatal
Subcortical band heterotopia
Autosomal recessive, Unknown, X-linked recessive
Submucosal cleft palate
Sugarman brachydactyly
Infancy, Neonatal
Supernumerary kidney
Neonatal
Supratip dysplasia
Not applicable
Neonatal
Supravalvular aortic stenosis
Autosomal dominant
All ages
Syndactyly type 1
Autosomal dominant
Antenatal, Infancy, Neonatal
Syndactyly type 2
Autosomal dominant
Infancy, Neonatal
Syndactyly type 3
Autosomal dominant
Infancy, Neonatal
Syndactyly type 4
Autosomal dominant
Infancy, Neonatal
Syndactyly type 5
Autosomal dominant
Infancy, Neonatal
Syndactyly type 8
Autosomal dominant, X-linked recessive
Tessier number 4 facial cleft
Unknown
Antenatal, Neonatal
Tessier number 5 facial cleft
Antenatal, Neonatal
Tessier number 6 facial cleft
Antenatal, Neonatal
Tessier number 7 facial cleft
Autosomal dominant
Antenatal, Neonatal
Testicular agenesis
Neonatal
Testicular regression syndrome
Autosomal recessive
Neonatal