Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Trichothiodystrophy
Autosomal recessive, X-linked recessive
Infancy, Neonatal
Trigeminal neuralgia
Not applicable
Adolescent, Adult, Elderly
Trigeminal trophic syndrome
Adult, Elderly
Triglyceride deposit cardiomyovasculopathy
Autosomal recessive, Unknown
Triose phosphate-isomerase deficiency
Autosomal recessive
Neonatal
Triple A syndrome
Autosomal recessive
All ages
Tritanopia
Autosomal dominant
Infancy, Neonatal
Tropical endomyocardial fibrosis
Not applicable
Adolescent, Adult, Childhood
Tropical pancreatitis
Childhood
Tropical spastic paraparesis
Not applicable
Adult
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
Tularemia
Not applicable
All ages
Tumor necrosis factor receptor 1 associated periodic syndrome
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Tungiasis
Not applicable
All ages
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
Tyrosinemia type 1
Autosomal recessive
All ages