Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Congenital primary megaureter, obstructed form
Unknown
Infancy, Neonatal
Congenital primary megaureter, refluxing and obstructed form
Infancy, Neonatal
Congenital primary megaureter, refluxing form
Unknown
Infancy, Neonatal
Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome
Autosomal recessive
Neonatal
Congenital pseudoarthrosis of the clavicle
Not applicable
Childhood, Infancy, Neonatal
Congenital ptosis
Autosomal dominant, X-linked recessive
Infancy, Neonatal
Congenital pulmonary airway malformation
Not applicable
Adolescent, Adult, Antenatal, Neonatal
Congenital pulmonary airway malformation type 0
Antenatal, Neonatal
Congenital pulmonary airway malformation type 1
Antenatal, Neonatal
Congenital pulmonary airway malformation type 2
Antenatal, Neonatal
Congenital pulmonary airway malformation type 3
Antenatal, Neonatal
Congenital pulmonary airway malformation type 4
Antenatal, Neonatal
Congenital pulmonary lymphangiectasia
Autosomal recessive
Neonatal
Congenital pulmonary sequestration
Neonatal
Congenital pulmonary valvar stenosis
Multigenic/multifactorial, Not applicable
Childhood, Infancy, Neonatal
Congenital pulmonary veins atresia or stenosis
Not applicable
Childhood
Congenital renal artery stenosis
Neonatal
Congenital respiratory-biliary fistula
Not applicable
Childhood
Congenital reticular ichthyosiform erythroderma
Autosomal dominant
Neonatal
Congenital retinal arteriovenous communication
Infancy, Neonatal
Congenital rubella syndrome
Not applicable
Antenatal, Neonatal
Congenital scalp aplasia cutis-enamel hypoplasia-developmental delay-intellectual disability syndrome
Autosomal dominant
Congenital secondary polycythemia
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Congenital short QT syndrome
Autosomal dominant
All ages