CSF1R, colony stimulating factor 1 receptor, 1436

N. diseases: 356; N. variants: 60
Disease: Hereditary Hyperexplexia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1835614
Disease: Hereditary Hyperexplexia
Hereditary Hyperexplexia 		0.010 GeneticVariation disease BEFREE The results provide strong evidence for genetic locus homogeneity and assign STHE to a 5.9-cM interval defined by CSF1-R and D5S379, which are separated by an RH map distance of 74 centirays (roughly 2.2-3.7 Mb). 1334371 1992