MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Denys-Drash syndrome

ORPHA:220Заболевание
Autosomal dominant

Dermatitis herpetiformis

ORPHA:1656Заболевание
Not applicable

Dermatofibrosarcoma protuberans

ORPHA:31112Заболевание
Not applicable

Dermatoleukodystrophy

ORPHA:1659Заболевание
Autosomal recessive

Dermatomyositis

ORPHA:221Заболевание
Not applicable

Dermatoosteolysis, Kirghizian type

ORPHA:1657Мальформация
Autosomal recessive

Dermatopathia pigmentosa reticularis

ORPHA:86920Заболевание
Autosomal dominant

Dermatosparaxis Ehlers-Danlos syndrome

ORPHA:1901Заболевание
Autosomal recessive

Dermochondrocorneal dystrophy

ORPHA:79149Заболевание
Autosomal recessive

Dermoid or epidermoid cyst of the central nervous system

ORPHA:530033Морф. аномалия

Dermoodontodysplasia

ORPHA:1660Мальформация
Autosomal dominant

Dermotrichic syndrome

ORPHA:99688Мальформация

Desbuquois syndrome

ORPHA:1425Мальформация
Autosomal recessive

Desmin-related myopathy with Mallory body-like inclusions

ORPHA:84132Заболевание
Autosomal recessive

Desminopathy

ORPHA:98909Заболевание
Autosomal dominant, Autosomal recessive

Desmoid tumor

ORPHA:873Заболевание
Not applicable, Unknown

Desmoplastic infantile astrocytoma/ganglioglioma

ORPHA:251940Заболевание
Not applicable

Desmoplastic small round cell tumor

ORPHA:83469Заболевание
Not applicable

Desmoplastic/nodular medulloblastoma

ORPHA:251863Гист. подтип
Not applicable

Desmosterolosis

ORPHA:35107Заболевание
Autosomal recessive

Developmental and epileptic encephalopathy with spike-wave activation in sleep

ORPHA:725Заболевание
Autosomal dominant, Not applicable

Developmental and speech delay due to SOX5 deficiency

ORPHA:313892Клин. подтип
Autosomal dominant, Not applicable

Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency

ORPHA:289307Заболевание
Autosomal recessive

Developmental delay with autism spectrum disorder and gait instability

ORPHA:329195Заболевание
Autosomal recessive