MDFIC

MyoD family inhibitor domain containing
OMIM: 614511, Gene2Phenotype

3 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 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 6.140 Latest signed off version: v6.0 (30 Apr 2025)	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 4.21 Latest signed off version: v4.0 (30 Apr 2025)	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