KIAA1217

KIAA1217
OMIM: 617367, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber KIAA1217 in Mendeliome


Version 1.3837

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Skeletal system disorder MONDO:0005172, KIAA1217-related