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Term:
autoimmune lymphoproliferative syndrome (DOID:6688)
Annotations: Rat: (9) Mouse: (9) Human: (10) Chinchilla: (9) Bonobo: (10) Dog: (10) Squirrel: (10) Pig: (10)
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 1  
advanced sleep phase syndrome 2  
advanced sleep phase syndrome 3  
agammaglobulinemia +   
age related macular degeneration 8  
Alagille syndrome  
alpha chain disease 
Alpha-2-Deficient Collagen Disease 
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity  
Alzheimer's disease 18  
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis +   
antiphospholipid syndrome +   
AQUAPORIN 1 DEFICIENCY  
ataxia telangiectasia +   
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune disease of exocrine system 
autoimmune disease of gastrointestinal tract +   
autoimmune disease of skin and connective tissue +   
autoimmune disease of the nervous system +   
autoimmune disease of urogenital tract +  
autoimmune hepatitis  
autoimmune hypersensitivity disease +   
Autoimmune Hypophysitis 
AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE  
Autoimmune Limbic Encephalitis 
autoimmune lymphoproliferative syndrome +   
Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY.
Autoimmune Progesterone Dermatitis 
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 1 multiple types  
cataract 10 multiple types  
cataract 11 multiple types +   
cataract 12 multiple types  
cataract 13 with adult i phenotype  
cataract 14 multiple types  
cataract 15 multiple types  
cataract 16 multiple types  
cataract 18  
cataract 2 multiple types  
cataract 20 multiple types  
cataract 21 multiple types  
cataract 23  
cataract 24 
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
cataract 29 
cataract 3 multiple types  
cataract 30  
cataract 31 multiple types  
cataract 33  
cataract 36  
cataract 37 
cataract 38  
cataract 41  
cataract 42  
cataract 43  
cataract 44  
cataract 45  
cataract 46 juvenile-onset  
Cataract 48  
cataract 5 multiple types  
cataract 7  
cataract 8 multiple types 
cataract 9 multiple types  
Cenani-Lenz syndactyly syndrome  
CHARGE syndrome  
cherubism +   
chromosomal disease +   
chronic NK-cell lymphocytosis 
Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia  
complement factor I deficiency  
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  
complex cortical dysplasia with other brain malformations 7  
congenital diarrhea +   
congenital hemolytic anemia +   
Congenital Hepatic Fibrosis  
congenital hypoplastic anemia +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
Congenital Pain Insensitivity +   
corneal opacification and other ocular anomalies +   
cryoglobulinemia +   
desquamative interstitial pneumonia  
Diabetes Mellitus, Congenital Autoimmune 
Dwarfism +   
Experimental Autoimmune Myocarditis  
Experimental Autoimmune Uveitis +   
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
FTDALS3  
FTDALS4  
Gardner-Diamond Syndrome 
Genetic Skin Diseases +   
Granuloma +   
hairy cell leukemia +   
heavy chain disease +  
hereditary angioedema +   
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
hyperimmunoglobulin syndrome +   
hypogonadotropic hypogonadism 5 with or without anosmia +   
IgA glomerulonephritis +   
Immunoblastic Lymphadenopathy  
IMMUNODEFICIENCY 31B  
Immunodeficiency 38, with Basal Ganglia Calcification  
infectious mononucleosis  
inherited blood coagulation disease +   
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Jaccoud's syndrome 
Kallmann syndrome +   
Kartagener syndrome  
Laminopathies  
Latent Autoimmune Diabetes in Adults  
Lennox-Gastaut syndrome  
Linear IgA Bullous Dermatosis 
lupus erythematosus +   
Lymphangiomyoma +   
lymphocytic leukemia +   
lymphoma +   
lymphoproliferative syndrome 1  
lymphoproliferative syndrome 2  
Lymphoproliferative Syndrome 3  
Macrophage Activation Syndrome  
Marek Disease 
Marfan syndrome +   
membranous glomerulonephritis  
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY  
monogenic disease +   
multiple myeloma +   
Multisystem Autoimmune Disease, Infantile-Onset +   
Multisystem Autoimmune Disease, with Facial Dysmorphism  
Nervous System Heredodegenerative Disorders +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
osteochondrodysplasia +   
Parotidomegaly, Hereditary Bilateral 
Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections 
pemphigus +   
plasmacytoma +   
platelet-type bleeding disorder 10  
POEMS syndrome 
polycystic kidney disease +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
pulmonary alveolar microlithiasis  
RASopathies  
Rh deficiency syndrome  
rheumatoid arthritis +   
rheumatoid arthritis interstitial lung disease 
Sacral Agenesis with Vertebral Anomalies  
sarcoidosis +   
Schnitzler syndrome  
Sezary's disease  
Spondyloenchondrodysplasia  
Tn polyagglutination syndrome  
Tumor Lysis Syndrome  
type 1 diabetes mellitus +   
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 ;   NCI:C37864 ;   ORDO:3261
Definition Sources: MESH:D056735, http://ghr.nlm.nih.gov/condition/autoimmune-lymphoproliferative-syndrome

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