Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Classical-like Ehlers-Danlos syndrome type 2
Autosomal recessive
Infancy, Neonatal
Clear cell adenocarcinoma of the ovary
Adult
Clear cell renal carcinoma
Not applicable
Adult, Elderly
Clear cell sarcoma of kidney
Not applicable
Adolescent, Adult, Childhood, Infancy
Coats disease
Not applicable
Childhood
Coats plus syndrome
Autosomal recessive
Childhood
Cobblestone lissencephaly without muscular or ocular involvement
Autosomal recessive
Childhood, Infancy
Cocaine intoxication
Not applicable
All ages
Coccidioidomycosis
Not applicable
All ages
Cockayne syndrome
Autosomal recessive
All ages
Cogan syndrome
Not applicable
Adolescent, Adult, Childhood
Cold agglutinin disease
Multigenic/multifactorial
Adult
Cold-induced sweating syndrome
Autosomal recessive
Adult, Childhood
Collecting duct carcinoma
Not applicable
Adult
Colobomatous macrophthalmia-microcornea syndrome
Autosomal dominant
Adolescent, Childhood, Elderly, Infancy
Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome
Autosomal dominant
Infancy, Neonatal
Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome
Autosomal recessive
Neonatal
Colorado tick fever
Not applicable
All ages
Combined deficiency of factor V and factor VIII
Autosomal recessive
All ages
Combined deficiency of factor VII and factor X
Adolescent, Adult, Childhood, Infancy, Neonatal
Combined hamartoma of the retina and retinal pigment epithelium
Not applicable
Childhood
Combined hepatocellular carcinoma and cholangiocarcinoma
Adult, Elderly
Combined immunodeficiency due to CARD11 deficiency
Autosomal recessive
Infancy, Neonatal
Combined immunodeficiency due to CD27 deficiency
Autosomal recessive
Adolescent, Adult, Childhood, Infancy