X-linked complicated spastic paraplegia type 1
Also known as: SPG1
Also known as: SPG1
Also known as: BORNHOLM eye disease, Bornholm eye disease, Bornholm eye disease, X-linked recessive, bed, myopia, high, with nonprogressive cone dysfunction
Also known as: COD1, CORDX1, X-linked cone dystrophy 1, X-linked cone-rod dystrophy type 1, cone dystrophy 1, X-linked, cone dystrophy X-linked 1, cone-rod dystrophy X-linked 1, cone-rod dystrophy, X-linked, 1, cone-rod dystrophy, X-linked, 1, X-linked recessive, cone-rod dystrophy, X-linked, type 1
Also known as: COD2, CORDX2, X-linked cone dystrophy 2, X-linked cone-rod dystrophy type 2, cone dystrophy 2, X-linked, cone dystrophy X-linked 2, cone dystrophy, progressive X-linked, 2, cone-rod dystrophy X-linked 2, cone-rod dystrophy, X-linked, 2
Also known as: CORDX3, X-linked cone-rod dystrophy type 3, cone-rod dystrophy X-linked 3, cone-rod dystrophy, X-linked, 3, cone-rod dystrophy, X-linked, 3, X-linked recessive, cone-rod dystrophy, X-linked, type 3
Also known as: Cgh, HTC2, Macias Flores-Garcia Cruz-Rivera syndrome, Macias-Flores Garcia-Cruz Rivera syndrome, chromosome Xq27.1 Interchromosomal insertion syndrome, chromosome Xq27.1 interchromosomal insertion syndrome, congenital generalised hypertrichosis, Macias-Flores type, congenital generalized hypertrichosis, Macias-Flores type, hCG, hypertrichosis congenital generalised X-linked, hypertrichosis congenital generalized X-linked, hypertrichosis, congenital generalised, hypertrichosis, congenital generalized, hypertrichosis, congenital generalized, X-linked dominant
Also known as: hemolytic anemia, congenital, X-linked, hemolytic anemia, congenital, X-linked, X-linked recessive
Also known as: X-linked CSNB, XLCSNB, congenital stationary night blindness, X-linked
Also known as: CND, Guizar-Vazquez Luengas-Munoz syndrome, Guízar Vázquez-Luengas-muñoz syndrome, bilateral corneal dermoids, corneal dermoids and short stature, corneal dystrophy epithelial-short stature syndrome, dermoids of cornea
Also known as: ATS-DL, Alport syndrome and diffuse leiomyomatosis, Alport syndrome with diffuse leiomyomatosis, DL-ATS, Xq22.3 microdeletion syndrome, chromosome Xq22.3 centromeric deletion syndrome, diffuse leiomyomatosis in Alport syndrome, leiomyomatosis, diffuse, with Alport syndrome, leiomyomatosis, esophageal and vulval, with nephropathy
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