Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Frontal encephalocele
Antenatal, Infancy, Neonatal
Frontal fibrosing alopecia
Adult
Frontofacionasal dysplasia
Neonatal
Frontometaphyseal dysplasia
Autosomal dominant, X-linked dominant
Neonatal
Frontonasal dysplasia
Not applicable
Antenatal, Neonatal
Frontonasal dysplasia-alopecia-genital anomalies syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome
Infancy, Neonatal
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome
Autosomal recessive
Antenatal, Neonatal
Frontorhiny
Autosomal recessive
Neonatal
Frontotemporal dementia
Autosomal dominant
Adult
Frontotemporal dementia with motor neuron disease
Autosomal dominant
Adult
Fructose-1,6-bisphosphatase deficiency
Autosomal recessive
All ages
Fryns syndrome
Autosomal recessive
Antenatal, Neonatal
Fryns-Smeets-Thiry syndrome
Childhood
Fuchs endothelial corneal dystrophy
Autosomal dominant, Multigenic/multifactorial, Not applicable
Adult
Fuchs heterochromic iridocyclitis
Adult
Fucosidosis
Autosomal recessive
Childhood, Infancy
Fuhrmann syndrome
Autosomal recessive
Infancy, Neonatal
Fukutin-related limb-girdle muscular dystrophy R13
Autosomal recessive
Infancy
Full NF2-related schwannomatosis
Autosomal dominant
All ages
Full schwannomatosis
Autosomal dominant
Adult, Elderly
Fumaric aciduria
Autosomal recessive
Infancy, Neonatal
Functional variant of Guillain-Barré syndrome
Multigenic/multifactorial, Not applicable
All ages
Functioning gonadotropic adenoma
Adult