Also known as: CHMP2B amyotrophic lateral sclerosis, CHMP2B-related amyotrophic lateral sclerosis, Dmt1, FTD3, amyotrophic lateral sclerosis caused by mutation in CHMP2B, amyotrophic lateral sclerosis, Chmp2B-related, dementia, familial nonspecific, frontotemporal dementia, chromosome 3-linked
Also known as: FTDALS8, frontotemporal dementia and/or amyotrophic lateral sclerosis 8
Also known as: FTD-ALS, FTD-MND, FTDALS, frontotemporal dementia with ALS, frontotemporal dementia with amyotrophic lateral sclerosis
Also known as: RTLA, rvFTD
Also known as: FHI, Fuch's heterochromic iridocyclitis, Fuchs heterochromic cyclitis, Fuchs heterochromic uveitis, Fuchs uveitis syndrome, Fuchs' heterochromic cyclitis, Fuchs' heterochromic uveitis
Also known as: Endoepithelial corneal dystrophy, FCED, FECD, Fuchs endothelial corneal dystrophy, Fuchs endothelial dystrophy, Fuchs' corneal dystrophy, Fuchs' endothelial corneal dystrophy, corneal dystrophy, Fuchs endothelial, late hereditary endothelial dystrophyEndoepithelial corneal dystrophy, FCED, FECD, Fuchs endothelial corneal dystrophy, Fuchs endothelial dystrophy, Fuchs' corneal dystrophy, Fuchs' endothelial corneal dystrophy, corneal dystrophy, Fuchs endothelial, late hereditary endothelial dystrophy
Also known as: Endoepithelial corneal dystrophy, FCED, FECD, Fuchs endothelial corneal dystrophy, Fuchs endothelial dystrophy, Fuchs' corneal dystrophy, Fuchs' endothelial corneal dystrophy, corneal dystrophy, Fuchs endothelial, late hereditary endothelial dystrophy
Also known as: Fuhrmann syndrome, Fuhrmann-Rieger-de Sousa syndrome, bowing of the femurs, aplasia or hypoplasia of the fibula, and digital anomalies, fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly, fibular hypoplasia or aplasia-femoral bowing-oligodactyly syndrome
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