CFEOM1, the most common type, is now known to be caused by one of several mutations in the KIF21A gene, while CFEOM2 is caused by mutations in the PHOX2A gene.
Cystic Fibrosis Foundation | cystic fibrosis | Congenital disorder | Cystic fibrosis transmembrane conductance regulator | Rhomboid muscles | Cystic Fibrosis | Cystic fibrosis | Congenital adrenal hyperplasia | Adductor muscles of the hip | X-linked congenital stationary night blindness | ''Spiral Expansion of Muscles in Action'', plaster, photograph published in 1914 and 1919, in ''Cubists and Post-Impressionism'', by Arthur Jerome Eddy | Leber's congenital amaurosis | Epaxial and hypaxial muscles | Cystic Fibrosis Trust | Congenital lacrimal duct obstruction | Congenital insensitivity to pain with anhidrosis | Congenital fiber type disproportion | congenital disorder | Congenital chloride diarrhea | congenital adrenal hyperplasia | Color plate by Jacques Gautier d'Agoty, showing some of the muscles of the head. Part of a series of illustrations from Myologie complete en couleur et grandeur naturelle (1746) with texts by French physician and anatomist Guichard Joseph Duverney |