TLX3, T cell leukemia homeobox 3, 30012

N. diseases: 34; N. variants: 0
Disease: Congenital central hypoventilation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		0.220 Biomarker disease BEFREE We therefore conclude that RNX is not a major gene for CCHS in human. 12548735 2003
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		0.220 Biomarker disease MGD Proper development of relay somatic sensory neurons and D2/D4 interneurons requires homeobox genes Rnx/Tlx-3 and Tlx-1. 12023301 2002
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		0.220 AlteredExpression disease BEFREE We conclude that RNX, and presumably its expression, are not altered in our index cases of CCHS. 12407709 2002
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		0.220 Biomarker disease MGD Rnx deficiency results in congenital central hypoventilation. 10700185 2000