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

Classical-like Ehlers-Danlos syndrome type 2

ORPHA:536532Kr.
Autosomal recessive

Clear cell adenocarcinoma of the ovary

ORPHA:398971Kr.

Clear cell renal carcinoma

ORPHA:319276Kr.
Not applicable

Clear cell sarcoma of kidney

ORPHA:457246Kr.
Not applicable

Coats disease

ORPHA:190Kr.
Not applicable

Coats plus syndrome

ORPHA:313838Kr.
Autosomal recessive

Cobblestone lissencephaly without muscular or ocular involvement

ORPHA:352682Kr.
Autosomal recessive

Cocaine intoxication

ORPHA:90068Kr.
Not applicable

Coccidioidomycosis

ORPHA:228123Kr.
Not applicable

Cockayne syndrome

ORPHA:191Kr.
Autosomal recessive

Cogan syndrome

ORPHA:1467Kr.
Not applicable

Cold agglutinin disease

ORPHA:56425Kr.
Multigenic/multifactorial

Cold-induced sweating syndrome

ORPHA:157820Kr.
Autosomal recessive

Collecting duct carcinoma

ORPHA:247203Kr.
Not applicable

Colobomatous macrophthalmia-microcornea syndrome

ORPHA:468672Kr.
Autosomal dominant

Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome

ORPHA:363741Kr.
Autosomal dominant

Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome

ORPHA:435930Kr.
Autosomal recessive

Colorado tick fever

ORPHA:83595Kr.
Not applicable

Combined deficiency of factor V and factor VIII

ORPHA:35909Kr.
Autosomal recessive

Combined deficiency of factor VII and factor X

ORPHA:600691Kr.

Combined hamartoma of the retina and retinal pigment epithelium

ORPHA:440727Kr.
Not applicable

Combined hepatocellular carcinoma and cholangiocarcinoma

ORPHA:529852Kr.

Combined immunodeficiency due to CARD11 deficiency

ORPHA:357237Kr.
Autosomal recessive

Combined immunodeficiency due to CD27 deficiency

ORPHA:238505Kr.
Autosomal recessive