MBL2

mannose binding lectin 2
OMIM: 154545, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red MBL2 in Mendeliome


Version 1.4851

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • {Chronic infections, due to MBL deficiency} 614372