MedGen for PMC (Select 1895832) - MedGen

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Links from PMC

Items: 5

Select item 401191.

Blood clot formation in any part of the carotid arteries. This may produce carotid stenosis or occlusion of the vessel, leading to transient ischemic attack; cerebral infarction; or amaurosis fugax. [from MONDO]

MedGen UID:: 40119
•Concept ID:: C0007274
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 211602.

Thrombotic disease

The formation of a blood clot in the lumen of a vessel or heart chamber; causes include coagulation disorders and vascular endothelial injury. [from NCI]

MedGen UID:: 21160
•Concept ID:: C0040053
•: Pathologic Function

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 1631053.

Inherited blood coagulation disorder

Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation. [from MONDO]

MedGen UID:: 163105
•Concept ID:: C0852077
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 70694.

Infectious mononucleosis

A clinical syndrome of fever, sore throat, fatigue, and lymphadenopathy caused by infection with the Epstein-Barr virus. Subsequent physical findings may include hepatomegaly, palatal petechiae, jaundice, uvular edema, and splenomegaly. [from NCI]