Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Cerebrooculonasal syndrome
Autosomal dominant
Antenatal, Neonatal
Cerebrotendinous xanthomatosis
Autosomal recessive
Infancy, Neonatal
Cernunnos-XLF deficiency
Autosomal recessive
Infancy, Neonatal
Cerulean cataract
Autosomal dominant
Childhood
Cervical hypertrichosis-peripheral neuropathy syndrome
Autosomal recessive
Childhood
Chapare hemorrhagic fever
All ages
Char syndrome
Autosomal dominant
Antenatal, Infancy, Neonatal
Charcot-Marie-Tooth disease type 1
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Charcot-Marie-Tooth disease type 1A
Autosomal dominant
Childhood
Charcot-Marie-Tooth disease type 1B
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Charcot-Marie-Tooth disease type 1C
Autosomal dominant
Adolescent, Adult, Childhood
Charcot-Marie-Tooth disease type 1D
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Charcot-Marie-Tooth disease type 1E
Autosomal dominant
Childhood, Infancy
Charcot-Marie-Tooth disease type 1F
Autosomal dominant
Childhood, Infancy
Charcot-Marie-Tooth disease type 2B1
Autosomal recessive
Childhood
Charcot-Marie-Tooth disease type 2B2
Autosomal recessive
Adult
Charcot-Marie-Tooth disease type 2B5
Autosomal recessive
Childhood, Infancy
Charcot-Marie-Tooth disease type 2H
Autosomal recessive
Childhood
Charcot-Marie-Tooth disease type 2P
Autosomal dominant, Autosomal recessive
Adolescent, Adult
Charcot-Marie-Tooth disease type 2R
Autosomal recessive
Infancy
Charcot-Marie-Tooth disease type 2S
Autosomal recessive
Adolescent, Adult, Childhood, Infancy
Charcot-Marie-Tooth disease type 2T
Autosomal recessive
Adult
Charcot-Marie-Tooth disease type 4
Autosomal recessive
Childhood, Infancy
Charcot-Marie-Tooth disease type 4A
Autosomal recessive
Infancy, Neonatal