Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Transcobalamin deficiency
Autosomal recessive
Infancy, Neonatal
Transgrediens et progrediens palmoplantar keratoderma
Childhood
Transient erythroblastopenia of childhood
Childhood, Infancy
Transient familial neonatal hyperbilirubinemia
Neonatal
Transient hyperammonemia of the newborn
Neonatal
Transient infantile hypertriglyceridemia and hepatosteatosis
Autosomal recessive
Infancy, Neonatal
Transient myeloproliferative syndrome
Not applicable
Antenatal, Neonatal
Transient neonatal diabetes mellitus
Autosomal dominant, Autosomal recessive, Not applicable
Antenatal, Neonatal
Transient neonatal multiple acyl-CoA dehydrogenase deficiency
Autosomal dominant
Infancy, Neonatal
Transient neonatal myasthenia gravis
Not applicable
Antenatal, Neonatal
Transient predisposition to invasive pyogenic bacterial infection
Autosomal recessive
Childhood
Transient pseudohypoaldosteronism
Not applicable
Infancy
Transient tyrosinemia of the newborn
Neonatal
Transitional cell carcinoma of the corpus uteri
Adult
Transketolase deficiency
Autosomal recessive
Infancy, Neonatal
Transposition of the great arteries
Multigenic/multifactorial, Not applicable
Infancy, Neonatal
Treacher-Collins syndrome
Autosomal dominant, Autosomal recessive
Antenatal, Neonatal
Trehalase deficiency
Autosomal dominant
Adolescent, Adult
Tremor-ataxia-central hypomyelination syndrome
Autosomal recessive
Childhood, Infancy
Tremor-nystagmus-duodenal ulcer syndrome
Neonatal
Trench fever
All ages
Trichinellosis
Not applicable
All ages
Tricho-dento-osseous syndrome
Autosomal dominant
Childhood
Tricho-retino-dento-digital syndrome
Autosomal dominant
Neonatal