Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Congenital esophageal stenosis
Adolescent, Childhood, Infancy, Neonatal
Congenital hereditary facial paralysis-variable hearing loss syndrome
Autosomal recessive
Infancy, Neonatal
Congenital laryngeal cyst
Infancy, Neonatal
Congenital lobar emphysema
Not applicable
Adult, Childhood, Infancy, Neonatal
Congenital megacalycosis
Unknown
All ages
Congenital microgastria
Antenatal, Infancy, Neonatal
Congenital pancreatic cyst
Unknown
Infancy, Neonatal
Congenital partial agenesis of pericardium
Not applicable
Congenital partial pulmonary venous return anomaly
Adolescent, Adult, Childhood, Infancy
Congenital patella dislocation
Infancy, Neonatal
Congenital portosystemic shunt
All ages
Congenital primary megaureter
Unknown
Adolescent, Adult, Childhood, Infancy, Neonatal
Congenital pulmonary valvar stenosis
Multigenic/multifactorial, Not applicable
Childhood, Infancy, Neonatal
Congenital respiratory-biliary fistula
Not applicable
Childhood
Congenital retinal arteriovenous communication
Infancy, Neonatal
Congenital short bowel syndrome
Autosomal recessive, X-linked recessive
Infancy, Neonatal
Congenital total pulmonary venous return anomaly
Not applicable
Neonatal
Congenital tracheal stenosis
Not applicable
Infancy, Neonatal
Congenital tracheomalacia
No data available
Infancy
Congenital tricuspid stenosis
Infancy, Neonatal
Congenital tricuspid valve dysplasia
Antenatal, Neonatal
Congenital unilateral hypoplasia of depressor anguli oris
Autosomal dominant
Neonatal
Congenital velopharyngeal incompetence
Autosomal dominant
Neonatal
Congenital vertical talus
Autosomal dominant
Infancy, Neonatal