Редкие (орфанные) заболевания
Полная база 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, препаратами и исследованиями.
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
Tritanopia
Autosomal dominant
Infancy, Neonatal
Tropical endomyocardial fibrosis
Not applicable
Adolescent, Adult, Childhood
Tropical pancreatitis
Childhood
Tropical spastic paraparesis
Not applicable
Adult
Tuberculosis
Not applicable
All ages
Tuberous sclerosis complex
Autosomal dominant
All ages
Tubular aggregate myopathy
Autosomal dominant
Adolescent, Adult, Childhood
Tubulinopathy-associated dysgyria
Autosomal dominant, Not applicable
Infancy
Tubulocystic renal cell carcinoma
Adult, Elderly
Tubulointerstitial nephritis and uveitis syndrome
Multigenic/multifactorial
Adolescent, Adult, Childhood, Elderly
Tufted angioma
Multigenic/multifactorial, Not applicable
All ages