Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Drug reaction with eosinophilia and systemic symptoms
Not applicable
All ages
Drug-induced autoimmune hemolytic anemia
Multigenic/multifactorial
All ages
Drug-induced localized lipodystrophy
All ages
Drug-induced lupus erythematosus
Not applicable
All ages
Dubin-Johnson syndrome
Autosomal recessive
Adolescent, Adult
Duchenne muscular dystrophy
X-linked recessive
Childhood
Dyggve-Melchior-Clausen disease
Autosomal recessive
Infancy
Dysbetalipoproteinemia
Autosomal dominant, Multigenic/multifactorial
Adolescent, Adult, Childhood, Elderly
Dyschromatosis symmetrica hereditaria
Autosomal dominant
Childhood
Dyschromatosis universalis hereditaria
Autosomal dominant, Autosomal recessive
Childhood, Infancy
Dysembryoplastic neuroepithelial tumor
Not applicable
All ages
Dysequilibrium syndrome
Autosomal recessive
Neonatal
Dysferlin-related limb-girdle muscular dystrophy R2
Autosomal recessive
Adolescent, Adult
Dyskeratosis congenita
Autosomal dominant, Autosomal recessive, X-linked recessive
Adolescent, Adult, Childhood, Infancy, Neonatal
Dysplasia of head of femur, Meyer type
Infancy, Neonatal
Dyssegmental dysplasia, Rolland-Desbuquois type
Antenatal, Neonatal
Dyssegmental dysplasia, Silverman-Handmaker type
Autosomal recessive
Antenatal, Neonatal
Dystonia 16
Autosomal recessive
Childhood, Infancy
Dystonia 28
Autosomal dominant
Childhood, Infancy
Dystonia-aphonia syndrome
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Dystonia-parkinsonism-hypermanganesemia syndrome
Autosomal recessive
Infancy
Dystrophic epidermolysis bullosa pruriginosa
Autosomal dominant, Autosomal recessive
Childhood
EAST syndrome
Autosomal recessive
Infancy, Neonatal
EBV-induced lymphoproliferative disease due to CARMIL2 deficiency
Autosomal recessive
Childhood