LAMC2, laminin subunit gamma 2, 3918

N. diseases: 602; N. variants: 66
Disease: Herlitz Disease ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 6 197 0.810 None 1.000 14 54 1992 2017