Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Triploidy syndrome
Not applicable, Unknown
Antenatal, Neonatal
Trismus-pseudocamptodactyly syndrome
Autosomal dominant
Infancy, Neonatal
Trisomy 10p syndrome
Infancy, Neonatal
Trisomy 12p syndrome
Not applicable, Unknown
Neonatal
Trisomy 13 syndrome
Not applicable, Unknown
Antenatal, Neonatal
Trisomy 17p syndrome
Not applicable, Unknown
Infancy, Neonatal
Trisomy 18 syndrome
Not applicable, Unknown
Antenatal, Neonatal
Trisomy 18p syndrome
Adolescent, Adult, Childhood, Infancy
Trisomy 1q syndrome
Antenatal, Neonatal
Trisomy 20p syndrome
Not applicable, Unknown
Infancy, Neonatal
Trisomy 4p syndrome
Antenatal, Infancy, Neonatal
Trisomy 5p syndrome
Not applicable, Unknown
Antenatal, Neonatal
Trisomy 8p syndrome
Antenatal, Neonatal
Trisomy 8q syndrome
Unknown
Neonatal
Trisomy 9p syndrome
Antenatal, Neonatal
Trisomy X syndrome
Not applicable
Childhood, Infancy
Turner syndrome
Not applicable, Unknown
Antenatal, Childhood, Infancy, Neonatal
Turnpenny-Fry syndrome
Autosomal dominant
Ulbright-Hodes syndrome
Autosomal recessive
Neonatal
Ulna hypoplasia-intellectual disability syndrome
Autosomal recessive
Infancy, Neonatal
Ulnar hypoplasia-split foot syndrome
Neonatal
Ulnar-mammary syndrome
Autosomal dominant
Adolescent, Antenatal, Infancy, Neonatal
Ulnar/fibula ray defect-brachydactyly syndrome
Autosomal dominant
Infancy, Neonatal
Umbilical cord ulceration-intestinal atresia syndrome
Unknown
Antenatal