Disease: WAGR Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206115
Disease: WAGR Syndrome
WAGR Syndrome 		0.040 Biomarker disease BEFREE These observations indicate that preaxial polydactyly may be another feature of the WAGR syndrome and suggest the existence of a related gene in the WAGR critical region or in its proximity. 15742368 2005
CUI: C0206115
Disease: WAGR Syndrome
WAGR Syndrome 		0.040 Biomarker disease BEFREE We report two monozygotic twins and a third, unrelated patient with WAGR syndrome and additional clinical features not usually associated with WAGR. 15779023 2005
CUI: C0206115
Disease: WAGR Syndrome
WAGR Syndrome 		0.040 GeneticVariation disease BEFREE Gene 239FB, transcribed extensively in fetal brain, was isolated from the chromosome 11p13 region associated with mental retardation component of the WAGR (Wilms tumor, aniridia, genitourinary anomalies, mental retardation) syndrome. 9266672 1997
CUI: C0206115
Disease: WAGR Syndrome
WAGR Syndrome 		0.040 GeneticVariation disease BEFREE To map the cytogenetic aberrations molecularly, we screened DNA from cell lines with known WAGR-related chromosome abnormalities for rearrangements with pulsed field gel (PFG) analysis using probes deleted from one chromosome 11 homolog of a WAGR patient. 2852160 1988