MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
60 diseases matched (Situation) Reset

5-fluorouracil poisoning

ORPHA:217064Situation
Not applicable

AIDS wasting syndrome

ORPHA:90081Situation
Not applicable

Acquired aneurysmal subarachnoid hemorrhage

ORPHA:90065Situation
Not applicable

Acquired hemophagocytic lymphohistiocytosis associated with malignant disease

ORPHA:158057Situation

Acute lung injury

ORPHA:178320Situation
Not applicable

Acute peripheral arterial occlusion

ORPHA:90064Situation
Not applicable

Acute poisoning by drugs with membrane-stabilizing effect

ORPHA:43119Situation
Not applicable

Acute radiation syndrome

ORPHA:454831Situation
Not applicable

Acute tricyclic antidepressant poisoning

ORPHA:43117Situation
Not applicable

Adenovirus infection in immunocompromised patients

ORPHA:91127Situation
Not applicable

Anal fistula

ORPHA:228113Situation
Not applicable

CAR T cell therapy-associated cytokine release syndrome

ORPHA:542323Situation

Cardiogenic shock

ORPHA:97292Situation
Not applicable

Central retinal vein occlusion

ORPHA:411527Situation
Not applicable

Colchicine poisoning

ORPHA:31824Situation
Not applicable

Complication after organ transplantation

ORPHA:306644Situation
Not applicable

Complication in hemodialysis

ORPHA:268316Situation
Not applicable

Complications after hematopoietic stem cell transplantation

ORPHA:90053Situation
Not applicable

Cyanide poisoning

ORPHA:466670Situation
Not applicable

Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk

ORPHA:137698Situation
Not applicable

De novo thrombotic microangiopathy after kidney transplantation

ORPHA:244275Situation

Digitalis poisoning

ORPHA:31828Situation
Not applicable

Drug or radiation exposure-related interstitial lung disease

ORPHA:264978Situation

Growing teratoma syndrome

ORPHA:314613Situation
Not applicable
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