FANCA, FA complementation group A, 2175

N. diseases: 211; N. variants: 206
Disease: Sjogren-Larsson Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037231
Disease: Sjogren-Larsson Syndrome
Sjogren-Larsson Syndrome 		0.010 Biomarker disease BEFREE Complementation analyses suggested that the deficiency in fatty alcohol oxidation in the FAA.K1A cells and the SLS fibroblasts is a result of lesions in homologous genes. 9295289 1997