LMNA, lamin A/C, 4000

N. diseases: 824; N. variants: 285
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome
0.300 GermlineCausalMutation disease ORPHANET Ovarian failure and dilated cardiomyopathy due to a novel lamin mutation. 19283854 2009