ASPN

asporin
OMIM: 608135, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red ASPN in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • {Lumbar disc degeneration} MIM#603932
  • {Osteoarthritis susceptibility 3} MIM#607850