CCT, cataract, congenital, total, 907

N. diseases: 75; N. variants: 0
Disease: Leiomyomatosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206654
Disease: Leiomyomatosis
Leiomyomatosis 		0.010 GeneticVariation disease BEFREE Hypothetically, the deletion extends beyond the 5' end and probably includes a second contiguous gene responsible for leiomyomatosis (the DL gene) and even a third one coding for congenital cataract (the CCT gene). 8238008 1993