Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia (DOID:0080319)
Annotations: Rat: (3) Mouse: (3) Human: (4) Chinchilla: (3) Bonobo: (4) Dog: (3) Squirrel: (3) Pig: (3)
Parent Terms Term With Siblings Child Terms
ABC Disease 
Acquired Pulmonary Alveolar Proteinosis 
Addison's disease +   
adrenoleukodystrophy +   
agammaglobulinemia +   
Aland Island eye disease  
Allan-Herndon-Dudley syndrome  
alpha chain disease 
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity  
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis +   
antisynthetase syndrome  
autoimmune disease of blood +   
autoimmune disease of cardiovascular system +   
autoimmune disease of endocrine system +   
autoimmune disease of exocrine system +   
autoimmune disease of gastrointestinal tract +   
autoimmune disease of musculoskeletal system +   
autoimmune disease of the nervous system +   
autoimmune disease of urogenital tract +   
Autoimmune Hypophysitis 
Autoimmune Interstitial Lung, Joint, and Kidney Disease  
autoimmune lymphoproliferative syndrome +   
Autoimmune Progesterone Dermatitis 
Barth syndrome +   
benign neoplasm +   
blue cone monochromacy  
Borjeson-Forssman-Lehmann syndrome  
Brunner syndrome  
Burkitt lymphoma +   
cancer +   
Castleman disease +   
CD40 ligand deficiency +   
Charcot-Marie-Tooth disease X-linked recessive 2 
Charcot-Marie-Tooth disease X-linked recessive 3 
Charcot-Marie-Tooth disease X-linked recessive 4  
Charcot-Marie-Tooth disease X-linked recessive 5  
Chromosomal Instability with Tissue-Specific Radiosensitivity 
CINCA syndrome  
CK syndrome  
Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia  
combined oxidative phosphorylation deficiency 6  
common variable immunodeficiency +   
congenital disorder of glycosylation Icc  
congenital disorder of glycosylation Iy  
congenital nongoitrous hypothyroidism 9  
congenital stationary night blindness 1A  
congenital stationary night blindness 2A  
Cutaneous Telangiectasia and Cancer Syndrome, Familial  
Cysts +   
Dent disease +   
Diabetes Mellitus, Congenital Autoimmune  
Diamond-Blackfan anemia 14 with mandibulofacial dysostosis  
DNA ligase IV deficiency  
Duchenne muscular dystrophy +   
ectodermal dysplasia 1 +   
epidermolysis bullosa acquisita 
Epstein-Barr virus hepatitis 
EPSTEIN-BARR VIRUS INSERTION SITE 1  
Experimental Autoimmune Myocarditis  
Experimental Autoimmune Uveitis +   
Experimental Neoplasms +   
factor VIII deficiency +   
familial Mediterranean fever +   
Fanconi anemia complementation group B  
FG syndrome +   
frontometaphyseal dysplasia 1  
Galloway-Mowat syndrome 2  
Gardner-Diamond Syndrome 
glycogen storage disease IXa  
glycogen storage disease IXd  
Good syndrome 
Granuloma +   
hairy cell leukemia +   
Hamartoma +   
heavy chain disease +  
hemophilia B  
Hereditary Neoplastic Syndromes +   
hereditary sensory neuropathy X-linked 
hereditary spastic paraplegia 16 
hereditary spastic paraplegia 2  
hereditary spastic paraplegia 34 
hypogonadotropic hypogonadism 1 with or without anosmia  
ichthyosis follicularis-alopecia-photophobia syndrome  
IgA glomerulonephritis +   
IgG4-related disease  
IGSF1 deficiency syndrome  
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  
Immunoblastic Lymphadenopathy  
immunodeficiency 14  
immunodeficiency 15A  
immunodeficiency 16  
immunodeficiency 23  
immunodeficiency 33  
immunodeficiency 34  
immunodeficiency 36  
immunodeficiency 37  
immunodeficiency 40  
immunodeficiency 46  
immunodeficiency 47  
immunodeficiency 50  
immunodeficiency 53  
immunodeficiency 56  
immunodeficiency 58  
immunodeficiency 60  
immunodeficiency 70  
immunodeficiency with hyper IgM type 3  
infectious mononucleosis  
isolated growth hormone deficiency type III  
Jaccoud's syndrome 
Joubert syndrome 10  
Keipert syndrome  
Kennedy's disease  
Latent Autoimmune Diabetes in Adults  
Lesch-Nyhan syndrome +   
leukocyte adhesion deficiency +   
Linear IgA Bullous Dermatosis 
Lymphangiomyoma +   
lymphoma +   
lymphoproliferative syndrome 1  
lymphoproliferative syndrome 2  
Lymphoproliferative Syndrome 3  
Macrophage Activation Syndrome  
Marek Disease 
MASA syndrome  
megalocornea +   
MEHMO syndrome  
membranous glomerulonephritis  
MEND syndrome  
methylmalonic acidemia and homocysteinemia cblX type  
midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis  
Mullegama-Klein-Martinez syndrome  
multiple congenital anomalies-hypotonia-seizures syndrome 2  
multiple myeloma +   
Multiple Primary Neoplasms +   
Multisystem Autoimmune Disease with Facial Dysmorphism  
Multisystem Autoimmune Disease, Infantile-Onset +   
NATURAL KILLER CELL ENTEROPATHY  
Neoplasms by Histologic Type +   
Neoplasms by Site +   
Neoplasms, Hormone-Dependent  
Neoplasms, Post-Traumatic 
Neoplasms, Radiation-Induced +   
Neoplasms, Second Primary  
Neoplastic Pregnancy Complications +   
Neoplastic Processes +   
Norrie disease  
occipital horn syndrome  
oculocerebrorenal syndrome +   
Opitz GBBB syndrome type I  
oral hairy leukoplakia 
osteogenesis imperfecta type 19  
Paganini-Miozzo syndrome  
Paraneoplastic Syndromes +   
Partington syndrome  
Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections 
Pelizaeus-Merzbacher disease +   
pemphigoid gestationis 
phosphoglycerate kinase 1 deficiency  
phosphoribosylpyrophosphate synthetase superactivity  
plasmacytoma +   
pre-malignant neoplasm +   
Prieto syndrome 
psoriasis +   
purine nucleoside phosphorylase deficiency  
Renpenning syndrome  
retinitis pigmentosa 23  
Ritscher-Schinzel syndrome 2  
sarcoidosis +   
severe congenital encephalopathy due to MECP2 mutation  
Sezary's disease  
Shukla-Vernon syndrome  
sideroblastic anemia 1  
Simpson-Golabi-Behmel syndrome type 1  
Simpson-Golabi-Behmel syndrome type 2  
Spondyloenchondrodysplasia  
spondyloepiphyseal dysplasia tarda +   
syndactyly type 8  
syndromic X-linked intellectual disability 17 
syndromic X-linked intellectual disability 5  
syndromic X-linked intellectual disability Claes-Jensen type  
syndromic X-linked intellectual disability Siderius type  
syndromic X-linked intellectual disability Snyder type  
syndromic X-linked intellectual disability Turner type  
T-Lymphocytopenia +   
Tn polyagglutination syndrome  
Tumor Lysis Syndrome  
Tumor Predisposition Syndrome  
type 1 diabetes mellitus +   
Van Esch-O'Driscoll syndrome  
Waisman syndrome  
Waldenstroem's macroglobulinemia  
Wilson-Turner syndrome  
Wiskott-Aldrich syndrome +   
Woods Black Norbury Syndrome 
X-linked Aarskog syndrome  
X-linked adrenal hypoplasia congenita  
X-linked agammaglobulinemia  
X-linked chondrodysplasia punctata 1  
X-linked chronic granulomatous disease  
X-linked chronic idiopathic intestinal pseudo-obstruction  
X-linked cone-rod dystrophy 3  
X-linked congenital hemolytic anemia  
X-linked deafness 5  
X-linked distal spinal muscular atrophy 3  
X-linked dyskeratosis congenita +   
X-linked dystonia-parkinsonism  
X-linked Emery-Dreifuss muscular dystrophy 1  
X-linked Emery-Dreifuss muscular dystrophy 6  
X-linked hyper IgM syndrome  
X-linked ichthyosis +   
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia  
A T cell deficiency that is characterized by CD4 lymphopenia, severe chronic viral infections, and defective T-lymphocyte activation in males and has_material_basis_in X-linked inheritance of mutations in the gene encoding magnesium transporter-1 (MAGT1). (DO)
X-linked intellectual developmental disorder 108  
X-linked juvenile retinoschisis 1  
X-linked keratosis follicularis spinulosa decalvans  
X-linked lymphoproliferative syndrome 1  
X-linked lymphoproliferative syndrome 2  
X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques  
X-linked myopathy with excessive autophagy  
X-linked nephrolithiasis type I  
X-linked properdin deficiency  
X-linked recessive hypophosphatemic rickets  
X-linked severe combined immunodeficiency  
X-linked sideroblastic anemia with ataxia  
X-linked spermatogenic failure 2  
X-linked spinal muscular atrophy 2  
X-linked spinocerebellar ataxia 1  
X-linked spinocerebellar ataxia 5 
X-linked thrombocytopenia with beta-thalassemia  
X-linked VACTERL association  

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.