Aarskog Syndrome ; Abidi Syndrome ; Adrenoleukodystrophy ; Ahmad Syndrome ; Aicardi Syndrome ; Allan-Herndon-Dudley Syndrome ; Alpha-Thalassemia Intellectual Disability (see also ATRX-Associated XLID) ; AP1S2-Associated XLID ; Apak Ataxia-Spastic Diplegia Syndrome ; Arena Syndrome (see Pelizaeus-Merzbacher Syndrome) ; Armfield Syndrome ; Arts Syndrome ; ARX-Associated XLID ; Ataxia-Deafness-Dementia, X-linked ; Atkin-Flaitz Syndrome ; ATRX-Associated XLID ; Bergia Cardiomyopathy ; Bertini Syndrome ; Borjeson-Forssman-Lehmann Syndrome ; Branchial Arch Syndrome, X-Linked ; Cantu Syndrome ; Carpenter-Waziri Syndrome (see also ATRX-Associated XLID) ; Cerebro-Cerebello-Coloboma Syndrome ; Cerebro-Oculo-Genital Syndrome ; Cerebro-Palato-Cardiac Syndrome (see also Renpenning Syndrome) ; Charcot-Marie-Tooth Neuropathy, Cowchock Variant ; Charcot-Marie-Tooth Neuropathy, Ionasescu Variant ; Chassaing-Lacombe Chondrodysplasia ; Christian Syndrome ; Christianson Syndrome ; Chudley-Lowry Syndrome (see also ATRX-Associated XLID) ; CK Syndrome ; Clark-Baraitser Syndrome ; Coffin-Lowry Syndrome ; Cornelia de Lange Syndrome, X-Linked ; Craniofacioskeletal ; Duchenne Muscular Dystrophy ; Dyskeratosis Congenita ; Epilepsy-Intellectual Disability in Females ; Fitzsimmons Syndrome ; FLNA-Associated XLID ; Fragile X Syndrome ; Giuffre-Tsukahara Syndrome ; Glycerol Kinase Deficiency ; Golabi-Ito-Hall Syndrome (see also Renpenning Syndrome) ; Goldblatt Spastic Paraplegia Syndrome ; Goltz Syndrome ; Graham Anophthalmia Syndrome ; Gustavson Syndrome ; Hall Orofacial Syndrome ; Hereditary Bullous Dystrophy, X-Linked ; Holmes-Gang Syndrome (see also ATRX-Associated XLID) ; Homfray Seizures-Contractures ; Hyde-Forster Syndrome ; Hydranencephaly with Abnormal Genitalia ; Hydrocephaly-Cerebellar Agenesis Syndrome ; Hydrocephaly-MASA Spectrum ; Hypoparathyroidism, X-Linked ; Incontinentia Pigmenti ; Juberg-Marsidi-Brooks ; Kang Syndrome ; Lenz Microphthalmia Syndrome ; Lesch-Nyhan Syndrome ; Lissencephaly and Abnormal Genitalia, X-Linked (see also ARX-Associated XLID) ; Lissencephaly, X-Linked ; Lowe Syndrome ; Lujan Syndrome ; MEHMO Syndrome ; Menkes Syndrome ; MIDAS Syndrome ; Miles-Carpenter Syndrome ; Mohr-Tranebjaerg Syndrome ; Monoamine Oxidase-A Deficiency ; Mucopolysaccharidosis IIA ; Myotubular Myopathy ; Nance-Horan Syndrome ; Norrie Disease ; Optic Atrophy, X-Linked ; Opitz FG Syndrome ; Oral-Facial-Digital Syndrome I ; Ornithine Transcarbamoylase Deficiency ; Otopalatodigital Syndrome I (see also FLNA-Associated XLID) ; Otopalatodigital Syndrome II (see also FLNA-Associated XLID) ; Paine Syndrome ; Pallister W Syndrome ; Partington Syndrome (see also ARX-Associated XLID) ; Pelizaeus-Merzbacher Syndrome ; Periventricular Nodular Heterotopia (see also FLNA-Associated XLID) ; Pettigrew Syndrome ; Phosphoglycerate Kinase Deficiency ; Plott Syndrome ; Porteous Syndrome (see also Renpenning Syndrome) ; PPM-X ; Prieto Syndrome ; Proud Syndrome (see also ARX-Associated XLID) ; Pyruvate Dehydrogenase Deficiency ; Renpenning Syndrome ; Rett Syndrome ; Rett-like Seizures-Hypotonia ; Roifman Syndrome ; Say-Meyer Syndrome ; Schimke Syndrome ; Shashi Syndrome ; Shrimpton Syndrome ; Simpson-Golabi-Behmel Syndrome ; Smith-Fineman-Myers Syndrome ; Snyder-Robinson Syndrome ; Stocco dos Santos Syndrome ; Stoll Syndrome ; Sutherland-Haan Syndrome (see also Renpenning Syndrome) ; Telecanthus-Hypospadias Syndrome ; Turner XLID ; Urban Syndrome ; VACTERL-Hydrocephalus Syndrome ; Vasquez Syndrome ; Waisman-Laxova Syndrome ; Warkany Syndrome ; Wieacker-Wolff Syndrome ; Wilson-Turner Syndrome ; Wittwer Syndrome ; XLID-Agenesis of the Corpus Callosum ; XLID-Arch Fingerprints-Hypotonia Syndrome (see also ATRX-Associated XLID) ; XLID-Ataxia-Apraxia ; XLID-Ataxia-Dementia ; XLID-Blindness-Seizures-Spasticity ; XLID-Choreoathetosis ; XLID-Choroideremia-Ectodermal Dysplasia ; XLID-Cleft Lip/Cleft Palate ; XLID-Epilepsy (XIDE) ; XLID-Hydrocephaly-Basal Ganglia Calcifications (see also AP1S2-Associated XLID) ; XLID-Hypogammaglobulinemia ; XLID-Hypogonadism-Tremor ; XLID-Hypospadias ; XLID-Hypotonia-Recurrent Infections ; XLID-Ichthyosis-Hypogonadism ; XLID-Infantile Spasms (see also ARX-Associated XLID) ; XLID-Isolated Growth Hormone Deficiency ; XLID-Macrocephaly ; XLID-Macrocephaly-Macroorchidism ; XLID-Microcephaly-Testicular Failure ; XLID-Nail Dystrophy-Seizures ; XLID-Nystagmus-Seizures ; XLID-Optic Atrophy ; XLID-Panhypopituitarism ; XLID-Precocious Puberty ; XLID-Psoriasis ; XLID-Retinitis Pigmentosa ; XLID-Rolandic Seizures ; XLID-Spastic Paraplegia, Type 7 ; XLID-Spastic Paraplegia-Athetosis ; XLID-Spondyloepimetaphyseal Dysplasia ; XLID-Thyroid Aplasia-Cutis Verticis Gyrata ; XLID-Thyroxine-Binding Globulin Deficiency ; Young-Hughes Syndrome ; Appendices ; I. Genes Involved in X-Linked Intellectual Disability (by order of discovery) ; II. XLID Syndromes with Microcephaly ; III. XLID Syndromes with Macrocephaly ; IV. XLID Syndromes with Ocular Anomalies and/or Visual Impairment ; V. XLID Syndrome with Hearing Loss ; VI. XLID Syndromes with Facial Clefting ; VII. XLID Syndromes with Cardiac Malformations or other Cardiovascular Abnormalities ; VIII. XLID Syndromes with Urogenital Anomalies ; IX. XLID Syndromes with Neuronal Migration Disturbance ; X. XLID Syndromes with Spastic Paraplegia ; XI. XLID Syndromes with Seizures ; XII. XLID Syndromes with Hypotonia ; XIII. XLID Syndromes Predominately Affecting Females ; XIV. Duplication of XLID Genes and Regions of the X Chromosome Genome ; XV. Non-Syndromal XLID Families ; XVI. X-Inactivation in Heterozygous Females