F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Infarction of spinal cord ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2314994
Disease: Infarction of spinal cord
Infarction of spinal cord 		0.010 GeneticVariation disease BEFREE We describe a healthy child heterozygous for this prothrombin mutation who had a spinal cord infarct with no other prothrombotic risk factors. 10356151 1999