Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
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Congenital factor II deficiency

An inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms.

Hepatomegaly

Abnormally increased size of the liver.

Total: 1

(per page)

PMID (PMCID)
20608021	MIXED_SAMPLE
	Budd-Chiari syndrome.
	Bane A, Kebede D. Ethiop Med J. 2010;48(2):169-75.
	A 16-year-old Ethiopian male patient presented with 18 months history of anasarca, anemia & hepatomegaly associated with hypoprothrombinemia, and diagnosed to have Budd-Chiari syndrome (BCS).