Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Oromandibular dystonia
Adolescent, Adult, Childhood, Elderly, Infancy
Osgood-Schlatter disease
Not applicable
Adolescent, Childhood
Ossification anomalies-psychomotor developmental delay syndrome
Infancy, Neonatal
Osteochondritis dissecans
Not applicable
All ages
Osteochondrosis of the metatarsal bone
Adolescent, Adult
Osteochondrosis of the tarsal bone
Adolescent, Childhood
Osteofibrous dysplasia
Autosomal dominant
Childhood, Infancy
Osteogenesis imperfecta
Autosomal dominant, Autosomal recessive, X-linked recessive
All ages
Osteopetrosis with renal tubular acidosis
Autosomal recessive
Infancy, Neonatal
Osteopetrosis-hypogammaglobulinemia syndrome
Autosomal recessive
Infancy, Neonatal
Osteoporosis-pseudoglioma syndrome
Autosomal recessive
Childhood
Osteosarcoma
Not applicable
Childhood
Osteosclerosis-ichthyosis-premature ovarian failure syndrome
Unknown
Adolescent, Adult
Ovarian dysgerminoma
Unknown
Adolescent
Ovarian fibroma
Not applicable
Adult
Ovarian fibrothecoma
Not applicable
Adult
Ovarian hyperstimulation syndrome
Not applicable
Adolescent, Adult
Overhydrated hereditary stomatocytosis
Autosomal dominant
Infancy, Neonatal
Overlap myositis
Not applicable
Adult
Oxoglutaric aciduria
Autosomal recessive
Neonatal
PANDAS
Not applicable
Childhood
PAPA syndrome
Autosomal dominant
Childhood
PAPASH syndrome
Adolescent, Adult
PASH syndrome
No data available
Adult