EIF3F

eukaryotic translation initiation factor 3 subunit F
OMIM: 603914, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green EIF3F in Mendeliome Version 1.3512	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Mental retardation, autosomal recessive 67, MIM# 618295
Green EIF3F in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.357	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes EIF3F-related neurodevelopmental disorder Mental retardation, autosomal recessive 67, MIM# 618295
Green EIF3F in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.267 Component of the following Super Panels: Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Mental retardation, autosomal recessive 67, MIM# 618295
Green EIF3F in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Mental retardation, autosomal recessive 67, MIM# 618295
Green EIF3F in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 0.278	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes EIF3F-related neurodevelopmental disorder Mental retardation, autosomal recessive 67, MIM# 618295
Green EIF3F in Fetal anomalies Version 1.465	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Intellectual developmental disorder, autosomal recessive 67- MIM#618295