CSF2, colony stimulating factor 2, 1437

N. diseases: 1028; N. variants: 7
Disease: Congenital cerebral hernia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		0.040 GeneticVariation disease BEFREE 78 (72.22%) cases had an associated encephalocele with the CSF leak. 31604132 2020
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		0.040 Biomarker disease BEFREE Patient age, sex, ethnicity, body mass index (BMI), location of CSF leak, recurrence of CSF leak, and presence of encephalocele(s) were recorded. 31157725 2019
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		0.040 Biomarker disease BEFREE The presence and laterality of middle cranial fossa pits (small bony defects containing CSF) and encephaloceles (brain parenchyma protrusion through osseous defects with or without bony remodeling) were recorded. 31780461 2019
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		0.040 Biomarker disease BEFREE Endoscope-assisted repair of CSF otorrhea and temporal lobe encephaloceles via keyhole craniotomy. 28799867 2018