Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Isolated right ventricular hypoplasia
Autosomal recessive, Not applicable
Infancy, Neonatal
Isolated small intestine duplication
Not applicable
Infancy, Neonatal
Isolated splenogonadal fusion
No data available
Antenatal, Neonatal
Isolated tetra-amelia
Antenatal
Isolated tibial hemimelia
Autosomal dominant, Autosomal recessive, Not applicable
Antenatal, Infancy, Neonatal
Isolated tracheoesophageal fistula
Not applicable
Neonatal
Isolated ulnar hemimelia
Infancy, Neonatal
Isolated unilateral hemispheric cerebellar hypoplasia
Infancy, Neonatal
Kommerell diverticulum
Not applicable
Laryngotracheoesophageal cleft
Autosomal dominant, Not applicable
Antenatal, Neonatal
Laubry-Pezzi syndrome
Infancy, Neonatal
Macrodactyly of fingers
Infancy, Neonatal
Macrodactyly of toes
Infancy, Neonatal
Median cleft lip/mandible
Not applicable
Neonatal
Mediastinal arteriovenous malformation
Not applicable
Medullary sponge kidney
Autosomal dominant, Not applicable
Adult, Childhood
Mesoaxial synostotic syndactyly with phalangeal reduction
Autosomal recessive
Infancy, Neonatal
Microlissencephaly
Autosomal recessive
Infancy, Neonatal
Microtia
Autosomal dominant, Autosomal recessive, Not applicable
Infancy, Neonatal
Middle aortic syndrome
Not applicable
Childhood
Midline cervical cleft
Not applicable
Mirror-image polydactyly
Morning glory disc anomaly
Childhood
Multicystic dysplastic kidney
Not applicable
Infancy, Neonatal