Conditions related to genes on the X chromosome

Genetics Home Reference includes these conditions related to genes on the X chromosome:

• Aarskog-Scott syndrome
• Allan-Herndon-Dudley syndrome
• Alport syndrome
• amelogenesis imperfecta
• androgenetic alopecia
• androgen insensitivity syndrome
• breast cancer
• Charcot-Marie-Tooth disease
• choroideremia
• Coffin-Lowry syndrome
• color vision deficiency
• congenital hemidysplasia with ichthyosiform erythroderma and limb defects
• Cornelia de Lange syndrome
• deafness-dystonia-optic neuronopathy syndrome
• Duchenne and Becker muscular dystrophy
• Emery-Dreifuss muscular dystrophy
• Fabry disease
• FG syndrome
• fragile X syndrome
• frontometaphyseal dysplasia
• glucose-6-phosphate dehydrogenase deficiency
• hemophilia
• hypohidrotic ectodermal dysplasia
• immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome
• incontinentia pigmenti
• Kallmann syndrome
• L1 syndrome
• Lenz microphthalmia syndrome
• Lesch-Nyhan syndrome
• Lowe syndrome
• McLeod neuroacanthocytosis syndrome
• Melnick-Needles syndrome
• Menkes syndrome
• 3-methylglutaconic aciduria
• mucopolysaccharidosis type II
• nonsyndromic deafness
• Norrie disease
• ocular albinism
• oculofaciocardiodental syndrome
• Opitz G/BBB syndrome
• ornithine transcarbamylase deficiency
• otopalatodigital syndrome type 1
• otopalatodigital syndrome type 2
• paroxysmal nocturnal hemoglobinuria
• Pelizaeus-Merzbacher disease
• periventricular heterotopia
• Rett syndrome
• Simpson-Golabi-Behmel syndrome
• spastic paraplegia type 2
• spinal and bulbar muscular atrophy
• Swyer syndrome
• Turner syndrome
• Wiskott-Aldrich syndrome
• X-linked adrenal hypoplasia congenita
• X-linked adrenoleukodystrophy
• X-linked agammaglobulinemia
• X-linked dystonia-parkinsonism
• X-linked hyper IgM syndrome
• X-linked juvenile retinoschisis
• X-linked lissencephaly
• X-linked myotubular myopathy
• X-linked severe combined immunodeficiency
• X-linked sideroblastic anemia
• X-linked spondyloepiphyseal dysplasia tarda

GeneCards provides a table of genes on the X chromosome and disorders related to those genes.