Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Follicular cholangitis and pancreatitis
Unknown
Adult
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
Formiminoglutamic aciduria
Autosomal recessive
Childhood
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
Fragile X-associated primary ovarian insufficiency
Frank-Ter Haar syndrome
Autosomal recessive
Antenatal, Neonatal
Frasier syndrome
Autosomal dominant
Adolescent, Adult, Childhood
Free sialic acid storage disease
Autosomal recessive
Antenatal, Infancy, Neonatal
Friedreich ataxia
Autosomal recessive
Adolescent, Childhood
Frontal fibrosing alopecia
Adult
Frontometaphyseal dysplasia
Autosomal dominant, X-linked dominant
Neonatal
Frontotemporal dementia with motor neuron disease
Autosomal dominant
Adult
Fructose-1,6-bisphosphatase deficiency
Autosomal recessive
All ages
Fuchs endothelial corneal dystrophy
Autosomal dominant, Multigenic/multifactorial, Not applicable
Adult
Fuchs heterochromic iridocyclitis
Adult
Fucosidosis
Autosomal recessive
Childhood, Infancy
Fukutin-related limb-girdle muscular dystrophy R13
Autosomal recessive
Infancy
Full NF2-related schwannomatosis
Autosomal dominant
All ages
Full schwannomatosis
Autosomal dominant
Adult, Elderly