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
Dermatoosteolysis, Kirghizian type
Autosomal recessive
Infancy
Dermatopathia pigmentosa reticularis
Autosomal dominant
Infancy, Neonatal
Dermatosparaxis Ehlers-Danlos syndrome
Autosomal recessive
Infancy, Neonatal
Dermochondrocorneal dystrophy
Autosomal recessive
Childhood
Dermoid or epidermoid cyst of the central nervous system
Adult
Dermoodontodysplasia
Autosomal dominant
Childhood
Dermotrichic syndrome
Neonatal
Desbuquois syndrome
Autosomal recessive
Antenatal, Neonatal
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
Desmoplastic/nodular medulloblastoma
Not applicable
Adult
Desmosterolosis
Autosomal recessive
Antenatal, Infancy, Neonatal
Developmental and epileptic encephalopathy with spike-wave activation in sleep
Autosomal dominant, Not applicable
Childhood
Developmental and speech delay due to SOX5 deficiency
Autosomal dominant, Not applicable
Infancy, Neonatal
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