MED14

mediator complex subunit 14
OMIM: 300182, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

No list MED14 in Mendeliome


Version 1.3053

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Literature
Phenotypes
  • Neurodevelopmental disorder (MONDO:0700092), MED14-related