MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов
Найдено 3,968 заболеваний (Заболевание)Сбросить

Drug reaction with eosinophilia and systemic symptoms

ORPHA:139402Заболевание
Not applicable

Drug-induced autoimmune hemolytic anemia

ORPHA:90037Заболевание
Multigenic/multifactorial

Drug-induced localized lipodystrophy

ORPHA:90157Заболевание

Drug-induced lupus erythematosus

ORPHA:231111Заболевание
Not applicable

Dubin-Johnson syndrome

ORPHA:234Заболевание
Autosomal recessive

Duchenne muscular dystrophy

ORPHA:98896Заболевание
X-linked recessive

Dyggve-Melchior-Clausen disease

ORPHA:239Заболевание
Autosomal recessive

Dysbetalipoproteinemia

ORPHA:412Заболевание
Autosomal dominant, Multigenic/multifactorial

Dyschromatosis symmetrica hereditaria

ORPHA:41Заболевание
Autosomal dominant

Dyschromatosis universalis hereditaria

ORPHA:241Заболевание
Autosomal dominant, Autosomal recessive

Dysembryoplastic neuroepithelial tumor

ORPHA:251946Заболевание
Not applicable

Dysequilibrium syndrome

ORPHA:1766Заболевание
Autosomal recessive

Dysferlin-related limb-girdle muscular dystrophy R2

ORPHA:268Заболевание
Autosomal recessive

Dyskeratosis congenita

ORPHA:1775Заболевание
Autosomal dominant, Autosomal recessive, X-linked recessive

Dysplasia of head of femur, Meyer type

ORPHA:168621Заболевание

Dyssegmental dysplasia, Rolland-Desbuquois type

ORPHA:156731Заболевание

Dyssegmental dysplasia, Silverman-Handmaker type

ORPHA:1865Заболевание
Autosomal recessive

Dystonia 16

ORPHA:210571Заболевание
Autosomal recessive

Dystonia 28

ORPHA:589618Заболевание
Autosomal dominant

Dystonia-aphonia syndrome

ORPHA:412217Заболевание
Autosomal dominant

Dystonia-parkinsonism-hypermanganesemia syndrome

ORPHA:521406Заболевание
Autosomal recessive

Dystrophic epidermolysis bullosa pruriginosa

ORPHA:89843Заболевание
Autosomal dominant, Autosomal recessive

EAST syndrome

ORPHA:199343Заболевание
Autosomal recessive

EBV-induced lymphoproliferative disease due to CARMIL2 deficiency

ORPHA:542301Заболевание
Autosomal recessive