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Ontology Browser

Term:
autoimmune lymphoproliferative syndrome (DOID:6688)
Annotations: Rat: (64) Mouse: (64) Human: (67) Chinchilla: (60) Bonobo: (61) Dog: (63) Squirrel: (59) Pig: (62)
Parent Terms Term With Siblings Child Terms
Acquired Pulmonary Alveolar Proteinosis 
Addison's disease +   
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 3  
agammaglobulinemia +   
age related macular degeneration 8  
alpha chain disease 
Alpha-2-Deficient Collagen 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  
Aquaporin 1 Deficiency 
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
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 +   
A hypersensitivity reaction type IV disease that is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes). It is characterized by the production of an abnormally large number of lymphocytes. Accumulation of excess lymphocytes results in enlargement of the lymph nodes, the liver, and the spleen. (DO)
Autoimmune Progesterone Dermatitis 
BOCKENHEIMER SYNDROME  
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
CADASIL +   
CAKUT2  
Castleman disease +   
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
chromosomal disease +   
chronic NK-cell lymphocytosis  
CINCA syndrome  
Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia  
common variable immunodeficiency +   
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
Congenital Hepatic Fibrosis  
Congenital Pain Insensitivity +   
cryoglobulinemia +   
desquamative interstitial pneumonia  
Diabetes Mellitus, Congenital Autoimmune  
Dwarfism +   
Experimental Autoimmune Uveitis +   
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
familial Mediterranean fever +   
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
Gardner-Diamond Syndrome 
Genetic Skin Diseases +   
Granuloma +   
hairy cell leukemia +   
heavy chain disease +  
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
hypogonadotropic hypogonadism 5 with or without anosmia +   
IgA glomerulonephritis +   
IgG4-related disease  
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  
Immunoblastic Lymphadenopathy  
Immunodeficiency 78 with Autoimmunity and Developmental Delay  
Immunodeficiency 85  
Immunodeficiency 87 and Autoimmunity  
Immunodeficiency 89 and Autoimmunity  
infectious mononucleosis  
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Jaccoud's syndrome 
Kallmann syndrome +   
Laminopathies +   
Lennox-Gastaut syndrome  
Linear IgA Bullous Dermatosis 
Lymphangiomyoma +   
lymphoma +   
lymphoproliferative syndrome 1  
lymphoproliferative syndrome 2  
Lymphoproliferative Syndrome 3  
Macrophage Activation Syndrome  
Marek Disease 
Marfan syndrome +   
membranous glomerulonephritis  
monogenic disease +   
multiple myeloma +   
Multisystem Autoimmune Disease with Facial Dysmorphism  
Multisystem Autoimmune Disease, Infantile-Onset +   
NATURAL KILLER CELL ENTEROPATHY  
Nervous System Heredodegenerative Disorders +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
osteochondrodysplasia +   
Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections 
plasmacytoma +   
POEMS syndrome 
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
Sacral Agenesis with Vertebral Anomalies  
sarcoidosis +   
Schnitzler syndrome  
Sezary's disease  
Spondyloenchondrodysplasia  
Tumor Lysis Syndrome  
VEXAS syndrome  
Waldenstroem's macroglobulinemia  
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia  
X-linked lymphoproliferative syndrome 1  
X-linked lymphoproliferative syndrome 2  
yellow nail syndrome +  

Synonyms
Exact Synonyms: ALPS ;   Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant ;   Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant ;   Autoimmune Lymphoproliferative Syndromes ;   Canale Smith syndromes ;   Canale-Smith syndrome
Narrow Synonyms: ALPS1A ;   ALPS1B ;   AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL DOMINANT AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IA ;   AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL RECESSIVE ;   AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IB
Primary IDs: MESH:D056735
Alternate IDs: OMIM:601859 ;   RDO:0001333
Xrefs: GARD:8686 ;   ICD10CM:D89.82 ;   ICD9CM:279.41 ;   NCI:C37864 ;   ORDO:3261
Definition Sources: http://ghr.nlm.nih.gov/condition/autoimmune-lymphoproliferative-syndrome "DO" "DO", MESH:D056735

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