Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1437
Gene Symbol: CSF2
CSF2
CUI: C0039144
Disease: Syringomyelia
Syringomyelia
0.070 Biomarker BEFREE As with syringomyelia associated with Chiari anomalies, the main goal of PSS surgery is to reestablish CSF flow across the area of obstruction. 31675698

2019

Entrez Id: 1437
Gene Symbol: CSF2
CSF2
CUI: C0039144
Disease: Syringomyelia
Syringomyelia
0.070 Biomarker BEFREE The chronic CSF leak led to acquired Chiari malformation (CM) with syringomyelia. 30074451

2018

Entrez Id: 1437
Gene Symbol: CSF2
CSF2
CUI: C0039144
Disease: Syringomyelia
Syringomyelia
0.070 Biomarker BEFREE OBJECTIVEIn patients with syringomyelia and type I Chiari malformation (CM-I) who have required reoperation because of persistent, recurrent, or expanding syrinx, the senior author placed a stent from the fourth ventricle to the cervical subarachnoid space in hopes of promoting circulation of CSF out of the ventricle and away from the central canal of the spinal cord. 30497207

2018

Entrez Id: 1437
Gene Symbol: CSF2
CSF2
CUI: C0039144
Disease: Syringomyelia
Syringomyelia
0.070 Biomarker BEFREE Syringomyelia is an abnormal cystic dilatation of the spinal cord caused by excessive accumulation of CSF (cerebrospinal fluid). 29316818

2018

Entrez Id: 1437
Gene Symbol: CSF2
CSF2
CUI: C0039144
Disease: Syringomyelia
Syringomyelia
0.070 Biomarker BEFREE Arachnoid veils appear to partially obstruct CSF flow, are significantly more prevalent in cases of CM-I with syringomyelia, and therefore may play a role in the pathophysiology of CM-I-associated syringomyelia. 29027876

2017

Entrez Id: 1437
Gene Symbol: CSF2
CSF2
CUI: C0039144
Disease: Syringomyelia
Syringomyelia
0.070 Biomarker BEFREE Imaging studies were analyzed by 2 board-certified neuroradiologists for the following features: 1) location of the deformity; 2) presence or absence of cord signal abnormality or syringomyelia; 3) visible arachnoid web; 4) presence of a dural defect; 5) nature of dorsal cord indentation (abrupt "scalpel sign" vs "C"-shaped); 6) focal ventral cord kink; 7) presence of the nuclear trail sign (endplate irregularity, sclerosis, and/or disc-space calcification that could suggest a migratory path of a herniated disc); and 8) visualization of a complete plane of CSF ventral to the deformity. 28338452

2017

Entrez Id: 1437
Gene Symbol: CSF2
CSF2
CUI: C0039144
Disease: Syringomyelia
Syringomyelia
0.070 Biomarker BEFREE CSF flow velocity in the spinal subarachnoid space of participants with syringomyelia was similar at different locations despite differences in syrinx size and locations. 28729294

2017