MATN2

matrilin 2
OMIM: 602108, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red MATN2 in Mendeliome


Version 2.336

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Syndromic disease, MONDO:0002254