MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Primary Sjögren disease

ORPHA:289390Kr.
Not applicable

Primary adult heart tumor

ORPHA:874Kr.
Not applicable

Primary anetoderma

ORPHA:228272Kr.
Not applicable

Primary angiitis of the central nervous system

ORPHA:140989Kr.
Not applicable

Primary biliary cholangitis

ORPHA:186Kr.
Multigenic/multifactorial, Unknown

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

ORPHA:562639Kr.

Primary bone lymphoma

ORPHA:314684Kr.

Primary central nervous system lymphoma

ORPHA:46135Kr.
Not applicable

Primary choroidal lymphoma

ORPHA:714046Kr.
Not applicable

Primary ciliary dyskinesia

ORPHA:244Kr.
Autosomal dominant, Autosomal recessive, X-linked recessive

Primary ciliary dyskinesia-retinitis pigmentosa syndrome

ORPHA:247522Kr.
X-linked recessive

Primary condylar hyperplasia

ORPHA:477781Kr.

Primary cutaneous anaplastic large cell lymphoma

ORPHA:300865Kr.

Primary cutaneous peripheral T-cell lymphoma not otherwise specified

ORPHA:86885Kr.
Not applicable

Primary cutaneous plasmacytosis

ORPHA:451602Kr.
Not applicable

Primary dystonia, DYT13 type

ORPHA:98807Kr.
Autosomal dominant

Primary dystonia, DYT17 type

ORPHA:370103Kr.
Autosomal recessive

Primary dystonia, DYT2 type

ORPHA:99657Kr.
Autosomal recessive

Primary dystonia, DYT21 type

ORPHA:306734Kr.
Autosomal dominant

Primary dystonia, DYT27 type

ORPHA:464440Kr.
Autosomal recessive

Primary dystonia, DYT4 type

ORPHA:98805Kr.
Autosomal dominant

Primary dystonia, DYT6 type

ORPHA:98806Kr.
Autosomal dominant

Primary effusion lymphoma

ORPHA:48686Kr.

Primary erythromelalgia

ORPHA:90026Kr.
Autosomal dominant