Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
0.200 Biomarker disease MGD Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse. 11799477 2002
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
0.200 Biomarker disease MGD Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy. 10579712 1999