omimdefinitions

| Mental retardation, X-linked syndromic, Turner type, 300706 (3)
| Kabuki syndrome 2, 300867 (3)
| Mental retardation syndrome, X-linked, Siderius type, 300263 (3)
| Stocco dos Santos X-linked mental retardation syndrome, 300434 (3)
| Mental retardation, X-linked 81 (2)
| {Graves disease, susceptibility to, X-linked} (2)
| {Diabetes mellitus, insulin-dependent, X-linked} (2)
| {Leber optic atrophy, susceptibility to} (2)
| ?Mental retardation, X-linked, syndromic 12 (2)
| Mental retardation, X-linked 20 (2)
| Prieto syndrome (2)
| [Social cognition] (2)
| {Migraine, familial typical, susceptibility to, 2} (2)
| {Mycobacerium tuberculosis, susceptibility, X-linked} (2)
| Mental retardation, X-linked 58, 300210 (3)
| Alopecia, androgenetic, 2 (2)
| Androgen insensitivity, 300068 (3)
| Spinal and bulbar muscular atrophy of Kennedy, 313200 (3)
| Androgen insensitivity, partial, with or without breast cancer, 312300 (3)
| * 313700 ANDROGEN RECEPTOR| AR
| Hypospadias 1, X-linked, 300633 (3)
| Osteopathia striata with cranial sclerosis, 300373 (3)
| Spastic paraplegia 16, X-linked, complicated (2)
| Wieacker-Wolf syndrome, 314580 (3)
| Craniofrontonasal dysplasia, 304110 (3)
| Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, 300486 (3)
| Menkes disease, 309400 (3)
| Occipital horn syndrome, 304150 (3)
| Spinal muscular atrophy, distal, X-linked 3, 300489 (3)
| Ectodermal dysplasia 1, hypohidrotic, X-linked, 305100 (3)
| Tooth agenesis, selective, X-linked 1, 313500 (3)
| Cleft palate with ankyloglossia, 303400 (3)
| ?Abruzzo-Erickson syndrome, 302905 (3)
| FG syndrome 3 (2)
| Mental retardation, X-linked 77 (2)
| Mental retardation, X-linked, syndromic 9 (2)
| Alpha-thalassemia/mental retardation syndrome, 301040 (3)
| Alpha-thalassemia myelodysplasia syndrome, somatic, 300448 (3)
| Mental retardation-hypotonic facies syndrome, X-linked, 309580 (3)
| Mental retardation, X-linked 93, 300659 (3)
| Wilson-Turner syndrome, 309585 (3)
| Cornelia de Lange syndrome 5, 300882 (3)
| Severe combined immunodeficiency, X-linked, 300400 (3)
| Combined immunodeficiency, X-linked, moderate, 312863 (3)
| Opitz-Kaveggia syndrome, 305450 (3)
| Lujan-Fryns syndrome, 309520 (3)
| Ohdo syndrome, X-linked, 300895 (3)
| {Autism susceptibility, X-linked 1}, 300425 (3)
| {Asperger syndrome susceptibility, X-linked 1}, 300494 (3)
| Phosphoglycerate kinase 1 deficiency, 300653 (3)
| Muscle glycogenosis, 300559 (3)
| Dystonia-Parkinsonism, X-linked, 314250 (3)
| Miles-Carpenter syndrome (2)
| Mental retardation, X-linked 90, 300850 (3)
| Charcot-Marie-Tooth neuropathy, X-linked dominant, 1, 302800 (3)
| Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia, 300853 (3)
| Anemia, sideroblastic, with ataxia, 301310 (3)
| Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia, 300472 (3)
| Myopathy, congenital, with fiber-type disproportion, X-linked (2)
| Mental retardation, X-linked 98, 300912 (3)
| Mental retardation, X-linked syndromic, Abidi type (2)
| Allan-Herndon-Dudley syndrome, 300523 (3)
| X-inactivation, familial skewed, 300087 (3)
| ?Mental retardation, X-linked 91, 300577 (3)
| Choroideremia, deafness, and mental retardation (4)
| Premature ovarian failure 2B, 300604 (3)
| Parkinson disease 12 (2)
| Aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies, 300887 (3)
| Metacarpal 4-5 fusion, 309630 (3)
| Deafness, X-linked 2, 304400 (3)
| Mental retardation, X-linked 97, 300803 (3)
| Choroideremia, 303100 (3)
| {Alzheimer disease 16} (2)
| Agammaglobulinemia, X-linked 1, 300755 (3)
| Agammaglobulinemia and isolated hormone deficiency, 307200 (3)
| Mental retardation, X-linked, syndromic, Chudley-Schwartz type, (2)
| Rolandic epilepsy, mental retardation, and speech dyspraxia, 300643 (3)
| Premature ovarian failure, 300511 (3)
| Fabry disease, 301500 (3)
| * 300644 GALACTOSIDASE, ALPHA| GLA
| Epileptic encephalopathy, early infantile, 9, 300088 (3)
| Pelizaeus-Merzbacher disease, 312080 (3)
| Spastic paraplegia 2, X-linked, 312920 (3)
| * 300356 TRANSLOCASE OF INNER MITOCHONDRIAL MEMBRANE 8, YEAST, HOMOLOG OF,
| Mohr-Tranebjaerg syndrome, 304700 (3)
| Jensen syndrome, 311150 (3)
| Gout, PRPS-related, 300661 (3)
| * 311850 PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE I| PRPS1
| Charcot-Marie-Tooth disease, X-linked recessive, 5, 311070 (3)
| Arts syndrome, 301835 (3)
| Deafness, X-linked 1, 304500 (3)
| ?Amelogenesis imperfecta, type IE, X-linked 2 (2)
| Epileptic encephalopathy, early infantile, 8, 300607 (3)
| Megalocornea 1, X-linked 309300 (3)
| Mental retardation, X-linked, syndromic, Martin-Probst type, 300519 (3)
| Thyroxine-binding globulin deficiency (3)
| Mental retardation, X-linked 53 (2)
| Mental retardation, X-linked 63, 300387 (3)
| Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis (4)
| Alport syndrome, 301050 (3)

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