Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Gorlin syndrome
Autosomal dominant
Adolescent, Adult
Grange syndrome
Autosomal dominant, Autosomal recessive
Childhood
Grant syndrome
Unknown
Neonatal
Greig cephalopolysyndactyly syndrome
Autosomal dominant
Antenatal
Greig cephalopolysyndactyly-contiguous gene syndrome
Antenatal
Growth delay-hydrocephaly-lung hypoplasia syndrome
Antenatal
Grubben-de Cock-Borghgraef syndrome
Antenatal, Neonatal
Guttmacher syndrome
Autosomal dominant
Infancy, Neonatal
Gómez-López-Hernández syndrome
Not applicable
Neonatal
H syndrome
Autosomal recessive
Childhood
HEC syndrome
Unknown
Neonatal
HIDEA syndrome
Autosomal recessive
Infancy, Neonatal
Haddad syndrome
Autosomal dominant, Multigenic/multifactorial
Infancy, Neonatal
Hajdu-Cheney syndrome
Autosomal dominant
Childhood, Infancy
Hall-Riggs syndrome
Autosomal recessive
Neonatal
Hallermann-Streiff syndrome
Not applicable, Unknown
Antenatal, Infancy, Neonatal
Hallermann-Streiff-like syndrome
Antenatal, Neonatal
Hallux varus-preaxial polysyndactyly syndrome
Neonatal
Hand-foot-genital syndrome
Autosomal dominant
Antenatal, Neonatal
Hardikar syndrome
X-linked dominant
Neonatal
Harrod syndrome
Infancy, Neonatal
Hartsfield syndrome
Autosomal dominant, Autosomal recessive
Antenatal
Hearing loss-familial salivary gland insensitivity to aldosterone syndrome
Infancy, Neonatal
Heart defect-tongue hamartoma-polysyndactyly syndrome
Autosomal recessive
Neonatal