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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы
Найдено 3,968 заболеваний (Disease) Сброс

Primary Sjögren disease

ORPHA:289390Disease
Not applicable

Primary adult heart tumor

ORPHA:874Disease
Not applicable

Primary anetoderma

ORPHA:228272Disease
Not applicable

Primary angiitis of the central nervous system

ORPHA:140989Disease
Not applicable

Primary biliary cholangitis

ORPHA:186Disease
Multigenic/multifactorial, Unknown

Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome

ORPHA:562639Disease

Primary bone lymphoma

ORPHA:314684Disease

Primary central nervous system lymphoma

ORPHA:46135Disease
Not applicable

Primary choroidal lymphoma

ORPHA:714046Disease
Not applicable

Primary ciliary dyskinesia

ORPHA:244Disease
Autosomal dominant, Autosomal recessive, X-linked recessive

Primary ciliary dyskinesia-retinitis pigmentosa syndrome

ORPHA:247522Disease
X-linked recessive

Primary condylar hyperplasia

ORPHA:477781Disease

Primary cutaneous anaplastic large cell lymphoma

ORPHA:300865Disease

Primary cutaneous peripheral T-cell lymphoma not otherwise specified

ORPHA:86885Disease
Not applicable

Primary cutaneous plasmacytosis

ORPHA:451602Disease
Not applicable

Primary dystonia, DYT13 type

ORPHA:98807Disease
Autosomal dominant

Primary dystonia, DYT17 type

ORPHA:370103Disease
Autosomal recessive

Primary dystonia, DYT2 type

ORPHA:99657Disease
Autosomal recessive

Primary dystonia, DYT21 type

ORPHA:306734Disease
Autosomal dominant

Primary dystonia, DYT27 type

ORPHA:464440Disease
Autosomal recessive

Primary dystonia, DYT4 type

ORPHA:98805Disease
Autosomal dominant

Primary dystonia, DYT6 type

ORPHA:98806Disease
Autosomal dominant

Primary effusion lymphoma

ORPHA:48686Disease

Primary erythromelalgia

ORPHA:90026Disease
Autosomal dominant