Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Dehydrated hereditary stomatocytosis
Autosomal dominant
Antenatal, Neonatal
Dejerine-Sottas syndrome
Autosomal dominant, Autosomal recessive, Not applicable
Infancy
Delayed encephalopathy due to carbon monoxide poisoning
All ages
Delayed membranous cranial ossification
Infancy, Neonatal
Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome
Childhood
Deletion 5q35 syndrome
Not applicable, Unknown
Antenatal, Neonatal
Delta-beta-thalassemia
Autosomal recessive
Infancy, Neonatal
Delta-sarcoglycan-related limb-girdle muscular dystrophy R6
Autosomal recessive
Childhood
Dementia pugilistica
Adult
Dengue fever
Not applicable
All ages
Dense deposit disease
Autosomal recessive
Childhood
Dent disease
X-linked recessive
Childhood
Dent disease type 1
X-linked recessive
Childhood
Dent disease type 2
X-linked recessive
Childhood, Infancy
Dental ankylosis
Adolescent, Adult, Childhood, Elderly
Dentatorubral pallidoluysian atrophy
Autosomal dominant
All ages
Dentin dysplasia
Autosomal dominant
All ages
Dentin dysplasia type I
Autosomal dominant, Autosomal recessive
Childhood
Dentin dysplasia type II
Autosomal dominant
Dentin dysplasia-sclerotic bones syndrome
Infancy
Dentinogenesis imperfecta
Autosomal dominant
Childhood
Dentinogenesis imperfecta type 2
Autosomal dominant
Childhood
Dentinogenesis imperfecta type 3
Autosomal dominant
Childhood
Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome
Autosomal recessive
Infancy, Neonatal