Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Fountain syndrome
Autosomal recessive
Infancy, Neonatal
Fowler vasculopathy
Autosomal recessive
Antenatal, Neonatal
Fragile X syndrome
X-linked dominant
Childhood, Infancy, Neonatal
Fragile X-associated tremor/ataxia syndrome
X-linked dominant
Adult
Fraser syndrome
Autosomal recessive
Antenatal, Neonatal
Freeman-Sheldon syndrome
Autosomal dominant, Autosomal recessive
Antenatal, Neonatal
Fried syndrome
X-linked recessive
Infancy, Neonatal
Fried's tooth and nail syndrome
Antenatal, Infancy, Neonatal
Frontofacionasal dysplasia
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
Fryns syndrome
Autosomal recessive
Antenatal, Neonatal
Fryns-Smeets-Thiry syndrome
Childhood
Fuhrmann syndrome
Autosomal recessive
Infancy, Neonatal
GAPO syndrome
Autosomal recessive
Neonatal
GMS syndrome
Neonatal
Gabriele-de Vries syndrome
Autosomal dominant
Antenatal, Neonatal
Galloway-Mowat syndrome
Autosomal recessive, X-linked recessive
Childhood, Infancy, Neonatal
Gastrointestinal tract arteriovenous malformation
Not applicable
Geleophysic dysplasia
Autosomal dominant, Autosomal recessive
Childhood
Gemignani syndrome
Autosomal recessive
Adult
Genitopalatocardiac syndrome
Antenatal, Neonatal