Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
ANE syndrome
Autosomal recessive
Adult
ANK3-related intellectual disability-sleep disturbance syndrome
Autosomal recessive
Childhood
AREDYLD syndrome
Autosomal recessive
Neonatal
ARX-related encephalopathy-brain malformation spectrum
Antenatal, Childhood, Infancy, Neonatal
ATP13A2-related parkinsonism
Adolescent, Childhood
ATP6AP1-CDG
X-linked recessive
Antenatal, Infancy, Neonatal
ATTRV122I amyloidosis
Autosomal dominant
Adult
ATTRV30M amyloidosis
Autosomal dominant
Adult
AXIN2-related polyposis
Autosomal dominant
Adult
Aarskog-Scott syndrome
Autosomal dominant, Autosomal recessive, X-linked recessive
Childhood
Aase-Smith syndrome type 1
Autosomal dominant
Antenatal, Neonatal
Abetalipoproteinemia
Autosomal recessive
Childhood, Infancy
Ablepharon macrostomia syndrome
Autosomal dominant
Antenatal, Neonatal
Abnormal origin of right or left pulmonary artery from the aorta
Infancy, Neonatal
Abruzzo-Erickson syndrome
X-linked recessive
Antenatal
Absence deformity of leg-cataract syndrome
Antenatal
Absence of fingerprints-congenital milia syndrome
Autosomal dominant
Childhood
Absence of the pulmonary artery
Not applicable
All ages
Absent radius-anogenital anomalies syndrome
Antenatal, Neonatal
Absent thumb-short stature-immunodeficiency syndrome
Unknown
Infancy, Neonatal
Absent tibia-polydactyly-arachnoid cyst syndrome
Unknown
Infancy, Neonatal
Acalvaria
Not applicable
Antenatal, Neonatal
Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome
Adult
Acatalasemia
Autosomal recessive
All ages