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Metadata
ID	GENO:0000149
Name	X-linked recessive inheritance
Synonyms	X-linked recessive inheritance [EXACT]
Parent Relationships	is_a X-linked inheritance
Related Diseases	has material basis in Barth syndrome X-linked sideroblastic anemia with ataxia Aland Island eye disease Allan-Herndon-Dudley syndrome blue cone monochromacy Borjeson-Forssman-Lehmann syndrome Dent disease X-linked myopathy with excessive autophagy congenital nonspherocytic hemolytic anemia 9 visceral heterotaxy 1 congenital disorder of glycosylation type IIr X-linked severe combined immunodeficiency CD40 ligand deficiency sideroblastic anemia 1 Kennedy's disease Renpenning syndrome MASA syndrome Simpson-Golabi-Behmel syndrome type 1 X-linked chondrodysplasia punctata 1 megalocornea orofaciodigital syndrome VIII Ritscher-Schinzel syndrome 2 Brunner Syndrome X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 X-linked juvenile retinoschisis 1 syndromic X-linked intellectual disability 5 MEHMO syndrome syndromic X-linked intellectual disability Snyder type syndromic X-linked intellectual disability 17 Prieto syndrome syndromic X-linked intellectual disability Claes-Jensen type syndromic X-linked intellectual disability Siderius type Wilson-Turner syndrome Wieacker-Wolff syndrome Norrie disease isolated growth hormone deficiency type III Holoprosencephaly 13, X-linked immunodeficiency 98 immunodeficiency 102 immunodeficiency 118 X-linked dyskeratosis congenita hereditary sensory neuropathy X-linked X-linked spermatogenic failure 2 X-linked chronic granulomatous disease X-linked Emery-Dreifuss muscular dystrophy 1 X-linked Emery-Dreifuss muscular dystrophy 6 X-linked spermatogenic failure 7 X-linked recessive disease multiple congenital anomalies-hypotonia-seizures syndrome 2 X-linked adrenal hypoplasia congenita developmental and epileptic encephalopathy 8 syndromic X-linked mental retardation 35 Galloway-Mowat syndrome 2 X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Simpson-Golabi-Behmel syndrome type 2 X-linked recessive hypophosphatemic rickets X-linked spondyloepiphyseal dysplasia tarda developmental and epileptic encephalopathy 1 congenital disorder of glycosylation Iy X-linked chronic idiopathic intestinal pseudo-obstruction Opitz GBBB syndrome X-linked keratosis follicularis spinulosa decalvans partial androgen insensitivity syndrome primary ovarian insufficiency 2B X-linked intellectual developmental disorder 109 syndromic X-linked intellectual disorder Lujan-Fryns-type X-linked nephrogenic diabetes insipidus ectodermal dysplasia and immunodeficiency 1 spastic paraplegia with deafness X-linked dystonia-parkinsonism hypogonadotropic hypogonadism 1 with or without anosmia immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 retinitis pigmentosa 23 hereditary spastic paraplegia 16 hereditary spastic paraplegia 2 hereditary spastic paraplegia 34 congenital stationary night blindness 1A congenital stationary night blindness 2A Joubert syndrome 10 X-linked cone-rod dystrophy 3 glycogen storage disease IXd glycogen storage disease IXa Fanconi anemia complementation group B IGSF1 deficiency syndrome X-linked distal spinal muscular atrophy 3 phosphoribosylpyrophosphate synthetase superactivity occipital horn syndrome combined oxidative phosphorylation deficiency 6 ectodermal dysplasia 1 X-linked deafness 5 X-linked VACTERL association X-linked thrombocytopenia with beta-thalassemia X-linked properdin deficiency Waisman syndrome frontometaphyseal dysplasia 1 X-linked nephrolithiasis type I syndactyly type 8 methylmalonic acidemia and homocysteinemia cblX type ichthyosis follicularis-alopecia-photophobia syndrome 1 X-linked spinal muscular atrophy 2 X-linked spinocerebellar ataxia 1 X-linked spinocerebellar ataxia 5 congenital nongoitrous hypothyroidism 9 congenital disorder of glycosylation Icc Van Esch-O'Driscoll syndrome Shukla-Vernon syndrome Keipert syndrome Paganini-Miozzo syndrome X-linked intellectual developmental disorder 108 X-linked congenital hemolytic anemia osteogenesis imperfecta type 19 midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis MEND syndrome Diamond-Blackfan anemia 14 with mandibulofacial dysostosis CK syndrome severe congenital encephalopathy due to MECP2 mutation phosphoglycerate kinase 1 deficiency immunodeficiency 34 immunodeficiency 50 immunodeficiency 47 immunodeficiency 33 X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques non-syndromic X-linked intellectual disability 73 non-syndromic X-linked intellectual disability 104 non-syndromic X-linked intellectual disability 103 non-syndromic X-linked intellectual disability ARX-related non-syndromic X-linked intellectual disability 21 non-syndromic X-linked intellectual disability 58 non-syndromic X-linked intellectual disability 99 non-syndromic X-linked intellectual disability 84 non-syndromic X-linked intellectual disability 92 non-syndromic X-linked intellectual disability 81 non-syndromic X-linked intellectual disability 9 non-syndromic X-linked intellectual disability 96 non-syndromic X-linked intellectual disability 105 non-syndromic X-linked intellectual disability 77 non-syndromic X-linked intellectual disability 100 non-syndromic X-linked intellectual disability 90 non-syndromic X-linked intellectual disability 93 non-syndromic X-linked intellectual disability 53 non-syndromic X-linked intellectual disability 101 non-syndromic X-linked intellectual disability 30 non-syndromic X-linked intellectual disability 82 non-syndromic X-linked intellectual disability 46 X-linked intellectual disability-short stature-overweight syndrome non-syndromic X-linked intellectual disability 72 X-Linked immunodeficiency 74 nuclear type mitochondrial complex I deficiency 30 nuclear type mitochondrial complex I deficiency 12 X-linked parkinsonism-spasticity syndrome nephrogenic syndrome of inappropriate antidiuresis HRPT-related hyperuricemia X-linked severe congenital neutropenia X-linked spondyloepimetaphyseal dysplasia X-linked dyserythropoietic anemia X-linked atrophic macular degeneration X-linked spermatogenic failure 3 oculocerebrorenal syndrome adrenoleukodystrophy Duchenne muscular dystrophy factor VIII deficiency hemophilia B X-linked agammaglobulinemia FG syndrome Partington syndrome X-linked ichthyosis Lesch-Nyhan syndrome glycogen storage disease VIII Pelizaeus-Merzbacher disease X-linked hyper IgM syndrome X-linked Aarskog syndrome Wiskott-Aldrich syndrome