MDFIC

MyoD family inhibitor domain containing
OMIM: 614511, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Green MDFIC in Fetal hydrops

Level 3: Fetal disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.95

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Nonimmune hydrops fetalis, HP:0001790
  • Lymphatic malformation 12, OMIM:620014
  • lymphatic malformation 12, MONDO:0031043
Green MDFIC in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 7.7
Latest signed off version: v7.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
  • Literature
Phenotypes
  • Lymphatic malformation 12, OMIM:620014
Amber MDFIC in Primary lymphoedema


Level 2: Cardiology
Version 5.1
Latest signed off version: v5.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Lymphatic malformation 12, OMIM:620014
  • lymphatic malformation 12, MONDO:0031043
Tags
  • Q4_25_promote_green
  • Q4_25_NHS_review