Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Complete hydatidiform mole
Autosomal recessive, Not applicable
Adult
Complex lethal osteochondrodysplasia
Autosomal recessive
Antenatal
Complex regional pain syndrome
Not applicable
All ages
Complex regional pain syndrome type 1
All ages
Complex regional pain syndrome type 2
All ages
Complication after organ transplantation
Not applicable
All ages
Complication in hemodialysis
Not applicable
All ages
Complications after hematopoietic stem cell transplantation
Not applicable
All ages
Composite hemangioendothelioma
Not applicable
All ages
Composite lymphoma
Adult, Elderly
Conductive deafness-malformed external ear syndrome
Unknown
Neonatal
Conductive deafness-ptosis-skeletal anomalies syndrome
No data available
Cone dystrophy with supernormal rod response
Autosomal recessive
Adolescent, Adult, Childhood
Cone rod dystrophy
Autosomal dominant, Autosomal recessive, X-linked recessive
Adolescent, Adult, Childhood
Cone rod dystrophy-short stature syndrome
Autosomal recessive
Childhood
Confetti-like macular atrophy
Adult
Congenital CLN10 disease
Autosomal recessive
Congenital Epstein-Barr virus infection
Not applicable
Infancy, Neonatal
Congenital Gerbode defect
Infancy, Neonatal
Congenital abducens nerve palsy
Not applicable
Neonatal
Congenital achiasma
Infancy, Neonatal
Congenital adrenal hyperplasia
Autosomal recessive
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
Autosomal recessive
Infancy, Neonatal
Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
Autosomal recessive
Infancy, Neonatal