Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Denys-Drash syndrome
Autosomal dominant
Adolescent, Childhood, Infancy, Neonatal
Dermatitis herpetiformis
Not applicable
All ages
Dermatofibrosarcoma protuberans
Not applicable
All ages
Dermatoleukodystrophy
Autosomal recessive
Neonatal
Dermatomyositis
Not applicable
Adult, Elderly
Dermatopathia pigmentosa reticularis
Autosomal dominant
Infancy, Neonatal
Dermatosparaxis Ehlers-Danlos syndrome
Autosomal recessive
Infancy, Neonatal
Dermochondrocorneal dystrophy
Autosomal recessive
Childhood
Desmin-related myopathy with Mallory body-like inclusions
Autosomal recessive
Infancy, Neonatal
Desminopathy
Autosomal dominant, Autosomal recessive
Adolescent, Adult, Childhood, Infancy
Desmoid tumor
Not applicable, Unknown
Adolescent, Adult
Desmoplastic infantile astrocytoma/ganglioglioma
Not applicable
Infancy, Neonatal
Desmoplastic small round cell tumor
Not applicable
Adolescent, Adult
Desmosterolosis
Autosomal recessive
Antenatal, Infancy, Neonatal
Developmental and epileptic encephalopathy with spike-wave activation in sleep
Autosomal dominant, Not applicable
Childhood
Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency
Autosomal recessive
Infancy, Neonatal
Developmental delay with autism spectrum disorder and gait instability
Autosomal recessive
Infancy, Neonatal
Developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome
Autosomal dominant
Infancy, Neonatal
Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome
Autosomal dominant
Childhood, Infancy
Diamond-Blackfan anemia
Autosomal dominant
Childhood, Infancy, Neonatal
Dianzani autoimmune lymphoproliferative disease
Unknown
All ages
Diaphyseal medullary stenosis-bone malignancy syndrome
Autosomal dominant
Diastrophic dysplasia
Autosomal recessive
Antenatal, Neonatal
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
Autosomal recessive
Infancy, Neonatal