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

Episodic ataxia type 7

ORPHA:209970Kr.
Autosomal dominant

Episodic ataxia with slurred speech

ORPHA:401953Kr.
Autosomal dominant

Epithelial basement membrane dystrophy

ORPHA:98956Kr.
Autosomal dominant

Epithelial recurrent erosion dystrophy

ORPHA:293381Kr.
Autosomal dominant

Epithelioid hemangioendothelioma

ORPHA:157791Kr.
Not applicable

Epithelioid hemangioma

ORPHA:675396Kr.

Epithelioid sarcoma

ORPHA:293202Kr.
Not applicable

Epithelioid trophoblastic tumor

ORPHA:254698Kr.
Not applicable

Epstein-Barr virus-associated gastric carcinoma

ORPHA:313920Kr.
Multigenic/multifactorial

Epstein-Barr virus-positive diffuse large B-cell lymphoma

ORPHA:289661Kr.
Not applicable

Erdheim-Chester disease

ORPHA:35687Kr.
Not applicable

Erosive pustular dermatosis of the scalp

ORPHA:222Kr.
Not applicable

Erythema elevatum diutinum

ORPHA:90000Kr.
Unknown

Erythema multiforme major

ORPHA:502499Kr.

Erythema palmare hereditarium

ORPHA:231031Kr.
Autosomal dominant

Erythroderma desquamativum

ORPHA:314Kr.
Autosomal recessive

Erythrokeratoderma ''en cocardes''

ORPHA:315Kr.
Autosomal dominant

Erythrokeratodermia variabilis

ORPHA:317Kr.
Autosomal dominant, Autosomal recessive

Erythrokeratodermia-cardiomyopathy syndrome

ORPHA:476096Kr.
Not applicable

Erythropoietic uroporphyria associated with myeloid malignancy

ORPHA:280379Kr.
Autosomal recessive

Essential fructosuria

ORPHA:2056Kr.
Autosomal recessive

Essential thrombocythemia

ORPHA:3318Kr.
Multigenic/multifactorial, Not applicable

Esthesioneuroblastoma

ORPHA:1957Kr.
Not applicable

Estrogen resistance syndrome

ORPHA:785Kr.
Autosomal recessive