Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Follicular dendritic cell sarcoma
All ages
Follicular lymphoma
Multigenic/multifactorial, Not applicable
Adult
Folliculotropic mycosis fungoides
Not applicable
Adult
Fontan-associated liver disease
Not applicable
Foodborne botulism
All ages
Formiminoglutamic aciduria
Autosomal recessive
Childhood
Fountain syndrome
Autosomal recessive
Infancy, Neonatal
Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome
Autosomal recessive
Neonatal
Foveal hypoplasia-presenile cataract syndrome
Autosomal dominant
Adult
Fowler urethral sphincter dysfunction syndrome
Unknown
Adolescent, Adult, Childhood
Fowler vasculopathy
Autosomal recessive
Antenatal, Neonatal
Fragile X syndrome
X-linked dominant
Childhood, Infancy, Neonatal
Fragile X-associated primary ovarian insufficiency
Fragile X-associated tremor/ataxia syndrome
X-linked dominant
Adult
Frank-Ter Haar syndrome
Autosomal recessive
Antenatal, Neonatal
Fraser syndrome
Autosomal recessive
Antenatal, Neonatal
Frasier syndrome
Autosomal dominant
Adolescent, Adult, Childhood
Free sialic acid storage disease
Autosomal recessive
Antenatal, Infancy, Neonatal
Free sialic acid storage disease, infantile form
Autosomal recessive
Antenatal, Neonatal
Freeman-Sheldon syndrome
Autosomal dominant, Autosomal recessive
Antenatal, Neonatal
Frey syndrome
Not applicable
Infancy
Fried syndrome
X-linked recessive
Infancy, Neonatal
Fried's tooth and nail syndrome
Antenatal, Infancy, Neonatal
Friedreich ataxia
Autosomal recessive
Adolescent, Childhood