Orphanet Database • Orphadata CC-BY-4.0
Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
7,547
Заболеваний
4 552
Генов
8 700
Фенотипов
140
Регионов
Все (7,547)Biological anomalyCategoryClinical groupClinical subtypeClinical syndromeDiseaseEtiological subtypeHistopathological subtypeMalformation syndromeMorphological anomalyParticular clinical situation in a disease or syndrome
Thyroid ectopia
Not applicable
Infancy, Neonatal
Thyroid hemiagenesis
Not applicable
Neonatal
Thyroid hypoplasia
Autosomal dominant, Not applicable
Infancy, Neonatal
Tracheal agenesis
Unknown
Antenatal, Neonatal
Tricuspid atresia
Not applicable
Antenatal, Neonatal
Uhl anomaly
Not applicable
Infancy, Neonatal
Unilateral ocular duplication
Autosomal dominant
Neonatal
Unilateral polymicrogyria
Infancy, Neonatal
Univentricular heart
Not applicable
Infancy, Neonatal
Urachal cyst
Not applicable
Infancy, Neonatal
Urachal diverticulum
Not applicable
Urachal sinus
Not applicable
Infancy, Neonatal
Vaginal atresia
Not applicable
Childhood
Vein of Galen malformation
Not applicable
Antenatal, Infancy, Neonatal
Williams-Campbell syndrome
Not applicable
Adult, Childhood