Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Thiamine-responsive encephalopathy
Autosomal recessive
Adolescent
Thiamine-responsive megaloblastic anemia syndrome
Autosomal recessive
Childhood
Thiel-Behnke corneal dystrophy
Autosomal dominant
Adolescent, Adult, Childhood
Thiemann disease, familial form
Not applicable
Adolescent
Thinking epilepsy
Thomsen and Becker disease
Autosomal dominant, Autosomal recessive
Adolescent, Adult, Childhood, Infancy
Thoracic outlet syndrome
Adult, Elderly
Thoracomelic dysplasia
Infancy
Thrombocythemia with distal limb defects
Autosomal dominant
Infancy, Neonatal
Thrombocytopenia with congenital dyserythropoietic anemia
X-linked recessive
Infancy, Neonatal
Thrombomodulin-related bleeding disorder
Autosomal dominant
All ages
Thrombotic thrombocytopenic purpura
Autosomal recessive, Multigenic/multifactorial
All ages
Thymic carcinoma
Not applicable
Adult
Thymic neuroendocrine carcinoma
Not applicable
Adult
Thymic neuroendocrine tumor
Adult, Elderly
Thymoma
Not applicable
Adult
Thymoma-hypogammaglobulinemia syndrome
Adult
Thyroid lymphoma
No data available
Thyrotoxic periodic paralysis
Multigenic/multifactorial, Not applicable
Adult
Tibial muscular dystrophy
Autosomal dominant, Autosomal recessive
Adult
Tick-borne encephalitis
Not applicable
All ages
Titin-related limb-girdle muscular dystrophy R10
Autosomal recessive
Adolescent, Adult, Childhood
Tolosa-Hunt syndrome
All ages
Torpedo Maculopathy
All ages