Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2153
Gene Symbol: F5
F5
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.040 GeneticVariation LHGDN The frequency of the fVL mutation in children with evidence of vascular thrombosis and their mothers was not statistically different from the frequency in children with CP with other imaging findings and their mothers. 16359589

2006
Entrez Id: 2153
Gene Symbol: F5
F5
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.040 GeneticVariation BEFREE The FVL mutation was found in 35% of the Arab CP patients (15/42) and in 22% of the controls from the same population (9/40) (P= 0.067). 16382706

2005
Entrez Id: 2153
Gene Symbol: F5
F5
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.040 GeneticVariation BEFREE Postoperative stroke in a child with cerebral palsy heterozygous for factor V Leiden. 10864060

2000
Entrez Id: 2153
Gene Symbol: F5
F5
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.040 GeneticVariation BEFREE A 5-year old girl with cerebral palsy (CP), preterm birth, postnatal aortic thrombus, and cerebellar venous infarction who is homozygous for the thrombophilic factor-V Leiden (fVL) mutation is reported. 10576642

1999