Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Endosteal hyperostosis, Worth type
Autosomal dominant
Adolescent
Endosteal sclerosis-cerebellar hypoplasia syndrome
Autosomal recessive
Infancy, Neonatal
Eng-Strom syndrome
Autosomal dominant
Antenatal
Enlarged parietal foramina
Autosomal dominant
Antenatal, Neonatal
Enteric anendocrinosis
Autosomal recessive
Infancy, Neonatal
Enteropathy-associated T-cell lymphoma
Not applicable
Adult
Enthesitis-related juvenile idiopathic arthritis
Unknown
Adolescent, Childhood
Eosinophilic angiocentric fibrosis
Not applicable
Adult
Eosinophilic colitis
Adult, Infancy
Eosinophilic cystitis
All ages
Eosinophilic fasciitis
Unknown
Adult
Eosinophilic gastroenteritis
Not applicable
All ages
Eosinophilic granulomatosis with polyangiitis
Not applicable
Adolescent, Adult, Elderly
Ependymal tumor
All ages
Ependymoma
Not applicable
All ages
Epibulbar lipodermoid-preauricular appendage-polythelia syndrome
Autosomal dominant
Infancy, Neonatal
Epidemic typhus
Not applicable
All ages
Epidermal nevus syndrome
Not applicable
Infancy, Neonatal
Epidermolysis bullosa acquisita
Not applicable
Adolescent, Adult, Childhood, Elderly, Infancy
Epidermolysis bullosa simplex
Autosomal dominant, Autosomal recessive
Adolescent, Childhood, Infancy, Neonatal
Epidermolysis bullosa simplex due to BP230 deficiency
Autosomal recessive
Adult
Epidermolysis bullosa simplex due to exophilin 5 deficiency
Autosomal recessive
Childhood
Epidermolysis bullosa simplex with anodontia/hypodontia
Infancy, Neonatal
Epidermolysis bullosa simplex with circinate migratory erythema
Autosomal dominant
Infancy, Neonatal