HLX, H2.0 like homeobox, 3142

N. diseases: 28; N. variants: 6
Disease: Congenital absence of spleen ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		0.010 Biomarker disease BEFREE HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia. 28898547 2017