X-Linked Recessive Disease

Disease ID: disease_node_13254

Connections displayed (default: 10).

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Subclassof	DOID_0050735
Data Source	DOID
Doid Label	X-linked recessive disease
Doid Description	A X-linked monogenic disease that has_material_basis_in recessive inheritance.
Disease Node Id	disease_node_13254
Doid Id	DOID_0080012
Label	X-Linked Recessive Disease

Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 73(ID:disease_node_16356) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Keratosis Follicularis Spinulosa Decalvans(ID:disease_node_19987) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Congenital Hemolytic Anemia(ID:disease_node_15282) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Lymphoproliferative Syndrome 1(ID:disease_node_20436) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Spermatogenic Failure 2(ID:disease_node_15220) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Intellectual Developmental Disorder 109(ID:disease_node_13599) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Emery-Dreifuss Muscular Dystrophy 6(ID:disease_node_18879) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Adrenal Hypoplasia Congenita(ID:disease_node_14163) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Intellectual Developmental Disorder 108(ID:disease_node_19232) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Juvenile Retinoschisis 1(ID:disease_node_16542) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Lymphoproliferative Syndrome 2(ID:disease_node_20429) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Spinocerebellar Ataxia 1(ID:disease_node_16061) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Immunodeficiency 74(ID:disease_node_20005) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Dystonia-Parkinsonism(ID:disease_node_14337) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Chronic Idiopathic Intestinal Pseudo-Obstruction(ID:disease_node_19436) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Spondyloepiphyseal Dysplasia Tarda(ID:disease_node_15692) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Atrophic Macular Degeneration(ID:disease_node_16563) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Chronic Granulomatous Disease(ID:disease_node_20424) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Vacterl Association(ID:disease_node_20212) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Emery-Dreifuss Muscular Dystrophy 1(ID:disease_node_18884) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Intellectual Disability-Short Stature-Overweight Syndrome(ID:disease_node_13594) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Sideroblastic Anemia With Ataxia(ID:disease_node_15250) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques(ID:disease_node_19369) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Myopathy With Excessive Autophagy(ID:disease_node_18987) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection, And Neoplasia(ID:disease_node_13308) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Nephrolithiasis Type I(ID:disease_node_19157) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Cone-Rod Dystrophy 3(ID:disease_node_16591) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Nephrogenic Diabetes Insipidus(ID:disease_node_19686) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Dyskeratosis Congenita(ID:disease_node_13630) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Spermatogenic Failure 3(ID:disease_node_15226) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Parkinsonism-Spasticity Syndrome(ID:disease_node_16707) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Dyserythropoietic Anemia(ID:disease_node_17081) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Recessive Hypophosphatemic Rickets(ID:disease_node_19038) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Deafness 5(ID:disease_node_19407) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Combined Immunodeficiency Diseases(ID:disease_node_11755) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Spermatogenic Failure 7(ID:disease_node_15184) (Disease)
Incoming r'ship SUBCLASS_OF to/from Wiskott-Aldrich Syndrome(ID:disease_node_7992) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic X-Linked Intellectual Disability Claes-Jensen Type(ID:disease_node_13614) (Disease)
Incoming r'ship SUBCLASS_OF to/from Wieacker-Wolff Syndrome(ID:disease_node_13609) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic X-Linked Intellectual Disability 17(ID:disease_node_13619) (Disease)
Incoming r'ship SUBCLASS_OF to/from Waisman Syndrome(ID:disease_node_20238) (Disease)
Incoming r'ship SUBCLASS_OF to/from Van Esch-O'Driscoll Syndrome(ID:disease_node_13592) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic X-Linked Mental Retardation 35(ID:disease_node_13603) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic X-Linked Intellectual Disability Snyder Type(ID:disease_node_13620) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic X-Linked Intellectual Disorder Lujan-Fryns-Type(ID:disease_node_13598) (Disease)
Incoming r'ship SUBCLASS_OF to/from Visceral Heterotaxy 1(ID:disease_node_19909) (Disease)
Incoming r'ship SUBCLASS_OF to/from Wilson-Turner Syndrome(ID:disease_node_13610) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 23(ID:disease_node_15831) (Disease)
Incoming r'ship SUBCLASS_OF to/from Simpson-Golabi-Behmel Syndrome Type 2(ID:disease_node_20307) (Disease)
Incoming r'ship SUBCLASS_OF to/from Shukla-Vernon Syndrome(ID:disease_node_20236) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ritscher-Schinzel Syndrome 2(ID:disease_node_19129) (Disease)
Incoming r'ship SUBCLASS_OF to/from Sideroblastic Anemia 1(ID:disease_node_15253) (Disease)
Incoming r'ship SUBCLASS_OF to/from Renpenning Syndrome(ID:disease_node_19229) (Disease)
Incoming r'ship SUBCLASS_OF to/from Prieto Syndrome(ID:disease_node_13617) (Disease)
Incoming r'ship SUBCLASS_OF to/from Pelizaeus-Merzbacher Disease(ID:disease_node_10558) (Disease)
Incoming r'ship SUBCLASS_OF to/from Paganini-Miozzo Syndrome(ID:disease_node_19233) (Disease)
Incoming r'ship SUBCLASS_OF to/from Partial Androgen Insensitivity Syndrome(ID:disease_node_14937) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 2B(ID:disease_node_17219) (Disease)
Incoming r'ship SUBCLASS_OF to/from Opitz Gbbb Syndrome(ID:disease_node_20283) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 53(ID:disease_node_16328) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 96(ID:disease_node_16339) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 46(ID:disease_node_16320) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability Arx-Related(ID:disease_node_16352) (Disease)
Incoming r'ship SUBCLASS_OF to/from Muscular Dystrophy, Duchenne(ID:disease_node_10569) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 99(ID:disease_node_16348) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 81(ID:disease_node_16341) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 90(ID:disease_node_16333) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 30(ID:disease_node_16981) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 84(ID:disease_node_16344) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 104(ID:disease_node_16355) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 103(ID:disease_node_16353) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 77(ID:disease_node_16335) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 92(ID:disease_node_16342) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nuclear Type Mitochondrial Complex I Deficiency 12(ID:disease_node_16980) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 21(ID:disease_node_16351) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 93(ID:disease_node_16330) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 101(ID:disease_node_16327) (Disease)
Incoming r'ship SUBCLASS_OF to/from Oculocerebrorenal Syndrome(ID:disease_node_5654) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 100(ID:disease_node_16334) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 72(ID:disease_node_16317) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 105(ID:disease_node_16338) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 58(ID:disease_node_16349) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2(ID:disease_node_16972) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 9(ID:disease_node_16340) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 82(ID:disease_node_16323) (Disease)
Incoming r'ship SUBCLASS_OF to/from Adrenoleukodystrophy(ID:disease_node_1035) (Disease)
Incoming r'ship SUBCLASS_OF to/from Barth Syndrome(ID:disease_node_12346) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bulbo-Spinal Atrophy, X-Linked(ID:disease_node_12066) (Disease)
Incoming r'ship SUBCLASS_OF to/from Blue Cone Monochromacy(ID:disease_node_19992) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cd40 Ligand Deficiency(ID:disease_node_13310) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Icc(ID:disease_node_20398) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Iy(ID:disease_node_20422) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ck Syndrome(ID:disease_node_16850) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease X-Linked Recessive 4(ID:disease_node_18823) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease X-Linked Recessive 5(ID:disease_node_18824) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency 6(ID:disease_node_16726) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 8(ID:disease_node_16193) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nonspherocytic Hemolytic Anemia 9(ID:disease_node_15263) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia 1, Anhidrotic(ID:disease_node_11687) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness 2A(ID:disease_node_20043) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ectodermal Dysplasia And Immunodeficiency 1(ID:disease_node_18091) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dent Disease(ID:disease_node_12450) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nongoitrous Hypothyroidism 9(ID:disease_node_14422) (Disease)
Incoming r'ship SUBCLASS_OF to/from Diamond-Blackfan Anemia 14 With Mandibulofacial Dysostosis(ID:disease_node_15307) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Stationary Night Blindness 1A(ID:disease_node_20044) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 1(ID:disease_node_16197) (Disease)
Incoming r'ship SUBCLASS_OF to/from Galloway-Mowat Syndrome 2(ID:disease_node_20287) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Type Viii(ID:disease_node_3537) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group B(ID:disease_node_15286) (Disease)
Incoming r'ship SUBCLASS_OF to/from Frontometaphyseal Dysplasia 1(ID:disease_node_15703) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Ixd(ID:disease_node_20396) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Ixa(ID:disease_node_20395) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hrpt-Related Hyperuricemia(ID:disease_node_17480) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 2(ID:disease_node_16635) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hypogonadotropic Hypogonadism 1 With Or Without Anosmia(ID:disease_node_17176) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hemophilia B(ID:disease_node_2097) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Sensory Neuropathy X-Linked(ID:disease_node_19421) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ichthyosis, X-Linked(ID:disease_node_8600) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Growth Hormone Deficiency Type Iii(ID:disease_node_19696) (Disease)
Incoming r'ship SUBCLASS_OF to/from Holoprosencephaly 13, X-Linked(ID:disease_node_13586) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 34(ID:disease_node_16694) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 50(ID:disease_node_13343) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hyper-Igm Immunodeficiency Syndrome, Type 1(ID:disease_node_11682) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Spastic Paraplegia 16(ID:disease_node_16639) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 47(ID:disease_node_13252) (Disease)
Incoming r'ship SUBCLASS_OF to/from Immunodeficiency 33(ID:disease_node_13342) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hemophilia A(ID:disease_node_3828) (Disease)
Incoming r'ship SUBCLASS_OF to/from Igsf1 Deficiency Syndrome(ID:disease_node_20251) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lesch-Nyhan Syndrome(ID:disease_node_4642) (Disease)
Incoming r'ship SUBCLASS_OF to/from Midface Hypoplasia, Hearing Impairment, Elliptocytosis, And Nephrocalcinosis(ID:disease_node_20386) (Disease)
Incoming r'ship SUBCLASS_OF to/from Megalocornea(ID:disease_node_18785) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mend Syndrome(ID:disease_node_16976) (Disease)
Incoming r'ship SUBCLASS_OF to/from Methylmalonic Acidemia And Homocysteinemia Cblx Type(ID:disease_node_19202) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 19(ID:disease_node_15635) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 30(ID:disease_node_16324) (Disease)
Outgoing r'ship SUBCLASS_OF to/from X-Linked Monogenic Disease(ID:disease_node_13360) (Disease)

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X-Linked Recessive Disease

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Disease Properties

Associated Connections 136

Disease Connections 136