Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Digital extensor muscle aplasia-polyneuropathy
Neonatal
Digitalis poisoning
Not applicable
All ages
Dihydropteridine reductase deficiency
Autosomal recessive
Infancy, Neonatal
Dihydropyrimidine dehydrogenase deficiency
Autosomal recessive
All ages
Dihydropyrimidinuria
Autosomal recessive
Childhood, Infancy
Dilated cardiomyopathy
All ages
Dilated cardiomyopathy with ataxia
Autosomal recessive
Childhood, Infancy
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
Autosomal recessive
Infancy, Neonatal
Dimethylglycine dehydrogenase deficiency
Autosomal recessive
Childhood
Diphallia
Infancy, Neonatal
Diphtheria
All ages
Diphyllobothriasis
Not applicable
All ages
Diprosopus
No data available
Antenatal
Dirofilariasis
Not applicable
All ages
Discoid lupus erythematosus
Adolescent, Adult, Childhood, Elderly
Dislocation of the hip-dysmorphism syndrome
Autosomal recessive
Infancy, Neonatal
Disorder of bile acid synthesis
All ages
Disorder of the gamma-glutamyl cycle
Autosomal recessive
Childhood, Infancy, Neonatal
Disorder of thiamine metabolism and transport
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Dissecting cellulitis of the scalp
Not applicable
Adult
Disseminated peritoneal leiomyomatosis
Unknown
Adult
Disseminated superficial actinic porokeratosis
Autosomal dominant
Adolescent, Adult, Childhood, Elderly
Distal 16p11.2 microdeletion syndrome
Not applicable
Antenatal, Infancy, Neonatal
Distal 17p13.1 microdeletion syndrome
Not applicable
Infancy, Neonatal