MYRF

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green MYRF in Anophthalmia_Microphthalmia_Coloboma Level 2: Ophthalmological disorders Version 1.39	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Nanophthalmos High hyperopia
Green MYRF in Congenital diaphragmatic hernia Level 2: Dysmorphic and congenital abnormality syndromes Version 1.14	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Cardiac-urogenital syndrome, MIM# 618280
Green MYRF in Differences of Sex Development Level 2: Dysmorphic and congenital abnormality syndromes Version 0.293	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes disorders of sex development
Green MYRF in Mendeliome Version 1.1902	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Nanophthalmos and high hyperopia Cardiac-urogenital syndrome, MIM# 618280 Encephalitis/encephalopathy, mild, with reversible myelin vacuolization, MIM# 618113
Green MYRF in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Expert list Phenotypes Cardiac-urogenital syndrome, MIM# 618280

5 panels