omimdefinitions

| ?Deafness, X-linked 6, 300914 (3)
| FG syndrome 5 (2)
| Lissencephaly, X-linked, 300067 (3)
| * 300121 DOUBLECORTIN| DCX
| Congenital disorder of glycosylation, type Is, 300884 (3)
| Tn polyagglutination syndrome, somatic, 300622 (3)
| Mental retardation, X-linked, syndromic 15 (Cabezas type), 300354 (3)
| Pyloric stenosis, infantile hypertrophic, 4 (2)
| Mental retardation, X-linked 30/47, 300558 (3)
| Bone mineral density QTL18, osteoporosis, 300910 (3)
| Mental retardation, X-linked 23 (2)
| {Obesity, susceptibility to, BMIQ11}, 300306 (3)
| {Coronary heart disease, susceptibility to, 3} (2)
| Myopia 13 (2)
| Deafness, X-linked 5 (2)
| Danon disease, 300257 (3)
| Mental retardation, X-linked, with short stature (2)
| * 300078 NADH-UBIQUINONE OXIDOREDUCTASE 1 ALPHA SUBCOMPLEX, 1| NDUFA1
| Mental retardation, X-linked 82 (2)
| Radial ray deficiency (2)
| Spastic paraplegia 34, X-linked (2)
| {Stature QTL 6} (2)
| Mental retardation, X-linked syndromic, Nascimento-type, 300860 (3)
| Albinism-deafness syndrome (2)
| Cowchock syndrome (2)
| Bazex syndrome (2)
| Ptosis, hereditary congenital 2 (2)
| Dermoids of cornea (2)
| Hypothyroidism, central, and testicular enlargement, 300888 (3)
| Lymphoproliferative syndrome, X-linked, 1, 308240 (3)
| Corneal dystrophy, endothelial, X-linked (2)
| Lymphoproliferative syndrome, X-linked, 2, 300635 (3)
| {Angioedema induced by ACE inhibitors, susceptibility to}, 300909 (3)
| Mental retardation, X-linked 94, 300699 (3)
| X inactivation, familial skewed, 2 (2)
| Mental retardation, X-linked, syndromic 14, 300676 (3)
| Thoracoabdominal syndrome (2)
| Pettigrew syndrome (2)
| Leukoencephalopathy with metaphyseal chondrodysplasia (2)
| Spinocerebellar ataxia, X-linked 5 (2)
| Mental retardation, X-linked 46, 300436 (3)
| Charcot-Marie-Tooth neuropathy, X-linked recessive, 3 (2)
| Simpson-Golabi-Behmel syndrome, type 1, 312870 (3)
| * 300037 GLYPICAN 3| GPC3
| Gustavson syndrome (2)
| Mental retardation, X-linked 42 (2)
| Split hand/foot malformation 2 (2)
| Immunodeficiency, X-linked, with hyper-IgM, 308230 (3)
| ?Craniofacioskeletal syndrome (2)
| Hypoparathyroidism, X-linked (2)
| Mental retardation, X-linked syndromic, Shashi type (2)
| Retinitis pigmentosa 24 (2)
| Lesch-Nyhan syndrome, 300322 (3)
| HPRT-related gout, 300323 (3)
| Wood neuroimmunologic syndrome (2)
| Combined oxidative phosphorylation deficiency 6, 300816 (3)
| * 300169 APOPTOSIS-INDUCING FACTOR, MITOCHONDRION-ASSOCIATED, 1| AIFM1
| Lowe syndrome, 309000 (3)
| Dent disease 2, 300555 (3)
| Mental retardation, X-linked syndromic, Raymond type, 300799 (3)
| Nystagmus 1, congenital, X-linked, 310700 (3)
| * 300628 FERM DOMAIN-CONTAINING PROTEIN 7| FRMD7
| Heterotaxy, visceral, 1, X-linked 306955 (3)
| * 300265 ZINC FINGER PROTEIN OF CEREBELLUM 3| ZIC3
| VACTERL association, X-linked, 314390 (3)
| Borjeson-Forssman-Lehmann syndrome, 301900 (3)
| Mental retardation, X-linked syndromic, Christianson type, 300243 (3)
| Mental retardation, X-linked, with isolated growth hormone deficiency, 300123 (3)
| Panhypopituitarism, X-linked, 312000 (3)
| 46XX sex reversal 3 (4)
| [Bone mineral density QTL 4] (2)
| Cone dystrophy, progressive X-linked, 2 (2)
| Testicular germ cell tumor (2)
| ?Microphthalmia, syndromic 4 (2)
| {Prostate cancer, hereditary, X-linked 1} (2)
| Microphthalmia, syndromic 1 (2)
| Hypertrichosis, congenital generalized (4)
| Hemophilia B, 306900 (3)
| * 300746 COAGULATION FACTOR IX| F9
| Thrombophilia, X-linked, due to factor IX defect, 300807 (3)
| {Deep venous thrombosis, protection against}, 300807 (3)
| Scapuloperoneal myopathy, X-linked dominant, 300695 (3)
| Myopathy, X-linked, with postural muscle atrophy, 300696 (3)
| Myopathy, reducing body, X-linked, severe early-onset, 300717 (3)
| Myopathy, reducing body, X-linked, childhood-onset, 300718 (3)
| * 300163 FOUR-AND-A-HALF LIM DOMAINS 1| FHL1
| Polymicrogyria, bilateral perisylvian (2)
| {Dyslexia, susceptibility to, 9} (2)
| Fragile X syndrome, 300624 (3)
| Fragile X tremor/ataxia syndrome, 300623 (3)
| Premature ovarian failure 1, 311360 (3)
| Chromosome Xq27.3-q28 duplication syndrome (4)
| Adrenoleukodystrophy, 300100 (3)
| * 300371 ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 1| ABCD1
| Mental retardation, X-linked, FRAXE type, 309548 (3)
| Deafness, dystonia, and cerebral hypomyelination, 300475 (3)
| Bornholm eye disease (2)
| * 300014 ATPase, Ca(2+)-TRANSPORTING, PLASMA MEMBRANE, 3| ATP2B3
| Diabetes insipidus, nephrogenic, 304800 (3)
| Nephrogenic syndrome of inappropriate antidiuresis, 300539 (3)

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