Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Carcinoma of gallbladder and extrahepatic biliary tract
Not applicable
Adult
Central congenital hypothyroidism
Central nervous system embryonal tumor
Not applicable
Childhood
Centronuclear myopathy
Autosomal dominant, Autosomal recessive, X-linked recessive
Adolescent, Adult, Childhood, Infancy, Neonatal
Cephalocele
Cerebral cortical dysplasia
Charcot-Marie-Tooth disease type 1
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Charcot-Marie-Tooth disease type 4
Autosomal recessive
Childhood, Infancy
Choroid plexus tumor
Chronic cutaneous lupus erythematosus
Multigenic/multifactorial
Adolescent, Adult, Childhood, Elderly
Cleft lip with or without cleft palate
Cleft palate
Multigenic/multifactorial, Not applicable
Antenatal, Neonatal
Cobblestone lissencephaly
Autosomal recessive
Infancy, Neonatal
Coenzyme Q10 deficiency
Autosomal recessive
All ages
Cold-induced sweating syndrome-hyperthermia spectrum
Autosomal recessive
Congenital adrenal hyperplasia
Autosomal recessive
Congenital dyserythropoietic anemia
Autosomal dominant, Autosomal recessive, X-linked recessive
Childhood
Congenital isolated hyperinsulinism
Autosomal dominant, Autosomal recessive
Childhood, Infancy, Neonatal
Congenital long QT syndrome
Autosomal dominant, Autosomal recessive
Adolescent, Adult, Childhood
Congenital myotonia
Congenital pulmonary veins atresia or stenosis
Not applicable
Childhood
Congenital stationary night blindness
Autosomal dominant, Autosomal recessive, X-linked recessive
Neonatal
Creatine deficiency syndrome
Autosomal recessive, Not applicable, X-linked recessive
Childhood, Infancy
Cutaneous mastocytosis
Not applicable
Childhood