Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Female infertility due to zona pellucida defect
Autosomal dominant, Autosomal recessive
Adult
Ferro-cerebro-cutaneous syndrome
X-linked recessive
Infancy
Ferroportin disease
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Autosomal recessive
Infancy, Neonatal
Fetal and neonatal alloimmune thrombocytopenia
Not applicable
Antenatal, Neonatal
Fetal cytomegalovirus syndrome
Not applicable
Antenatal, Neonatal
Fever-associated acute infantile liver failure syndrome
Autosomal recessive
Infancy
Fibroblastic rheumatism
Adolescent, Adult, Childhood
Fibrochondrogenesis
Autosomal dominant, Autosomal recessive
Neonatal
Fibrodysplasia ossificans progressiva
Autosomal dominant, Not applicable
Childhood
Fibrolamellar hepatocellular carcinoma
Not applicable
Adolescent, Adult
Fibronectin glomerulopathy
Autosomal dominant
All ages
Fibrosarcoma
Not applicable
All ages
Fibrosis-neurodegeneration-cerebral angiomatosis syndrome
Infancy, Neonatal
Fingerprint body myopathy
Neonatal
Fixed drug eruption
Not applicable
All ages
Fleck corneal dystrophy
Autosomal dominant
All ages
Florid cemento-osseous dysplasia
Not applicable
Adult
Flynn-Aird syndrome
Autosomal dominant
Childhood
Focal epilepsy-intellectual disability-cerebro-cerebellar malformation
Autosomal recessive
Infancy
Focal myositis
Not applicable
Adult
Focal palmoplantar and gingival keratoderma
Childhood
Focal palmoplantar keratoderma with joint keratoses
Autosomal dominant
Infancy, Neonatal
Folinic acid-responsive seizures
Unknown
Infancy, Neonatal