MED16

mediator complex subunit 16
OMIM: 604062, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber MED16 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.31
Latest signed off version: v8.0 (12 Aug 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Amber
Phenotypes
  • Guillouet-Gordon syndrome, MONDO:0979227
  • Guillouet-Gordon syndrome, OMIM:621220
Tags
  • Q3_26_promote_green
Green MED16 in Clefting


Level 2: Musculoskeletal
Version 7.22
Latest signed off version: v7.8 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Guillouet-Gordon syndrome, OMIM:621220
    Green MED16 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.86
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Guillouet-Gordon syndrome, OMIM:621220