Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Tularemia
Not applicable
All ages
Tumor necrosis factor receptor 1 associated periodic syndrome
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Tumor of cranial and spinal nerves
Tumor of endocrine glands
Tumor of testis and paratestis
Tungiasis
Not applicable
All ages
Turner syndrome
Not applicable, Unknown
Antenatal, Childhood, Infancy, Neonatal
Turner syndrome due to structural X chromosome anomalies
Antenatal, Childhood, Infancy, Neonatal
Turnpenny-Fry syndrome
Autosomal dominant
Twin anemia-polycythemia sequence
Antenatal
Twin-reversed arterial perfusion sequence
Antenatal
Typhoid
Not applicable
All ages
Typical nemaline myopathy
Autosomal dominant, Autosomal recessive
Antenatal, Neonatal
Typical urticaria pigmentosa
Autosomal dominant, Unknown
Tyrosinemia type 1
Autosomal recessive
All ages
Tyrosinemia type 2
Autosomal recessive
Adolescent, Childhood, Infancy, Neonatal
Tyrosinemia type 3
Autosomal recessive
Infancy, Neonatal
UMOD-related autosomal dominant tubulointerstitial kidney disease
Autosomal dominant
Adolescent, Adult
UV-sensitive syndrome
Autosomal recessive
Infancy
Uhl anomaly
Not applicable
Infancy, Neonatal
Ulbright-Hodes syndrome
Autosomal recessive
Neonatal
Ulerythema ophryogenesis
Autosomal dominant, Not applicable
Childhood
Ullrich congenital muscular dystrophy
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Ulna hypoplasia-intellectual disability syndrome
Autosomal recessive
Infancy, Neonatal