MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Parent Node:
expandintellectual disability (MONDO:0001071)
Parent Node:
expandsyndromic disease (MONDO:0002254)
..Starting node
..expandsyndromic intellectual disability ()

       Child Nodes:
........expandacrocallosal syndrome ()
........expandacrofacial dysostosis Rodriguez type ()
........expandacrofacial dysostosis, Catania type ()
........expandagnathia-otocephaly complex ()
........expandalopecia - contractures - dwarfism - intellectual disability syndrome ()
........expandalopecia - intellectual disability syndrome ()
........expandalopecia-epilepsy-pyorrhea-intellectual disability syndrome ()
........expandalpha thalassemia-intellectual disability syndrome type 1 ()
........expandAngelman syndrome ()
........expandaniridia-cerebellar ataxia-intellectual disability syndrome ()
........expandaniridia-renal agenesis-psychomotor retardation syndrome ()
........expandaortic arch anomaly-facial dysmorphism-intellectual disability syndrome ()
........expandatelosteogenesis type III ()
........expandBannayan-Riley-Ruvalcaba syndrome ()
........expandBiemond syndrome type 2 ()
........expandblepharonasofacial malformation syndrome ()
........expandBowen-Conradi syndrome ()
........expandBranchioskeletogenital syndrome ()
........expandc syndrome ()
........expandcardiocranial syndrome, Pfeiffer type ()
........expandcataract-hypertrichosis-intellectual disability syndrome ()
........expandcataract-intellectual disability-hypogonadism syndrome ()
........expandcataract-nephropathy-encephalopathy syndrome ()
........expandcerebrofaciothoracic dysplasia ()
........expandCharcot-Marie-Tooth disease-deafness-intellectual disability syndrome ()
........expandCohen syndrome ()
........expandcortical blindness-intellectual disability-polydactyly syndrome ()
........expandCostello syndrome ()
........expandCrane-Heise syndrome ()
........expandCzeizel-Losonci syndrome ()
........expanddelayed speech-facial asymmetry-strabismus-ear lobe creases syndrome ()
........expanddown syndrome ()
........expandDubowitz syndrome ()
........expandfacial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome ()
........expandfloating-Harbor syndrome ()
........expandGMS syndrome ()
........expandhepatic fibrosis-renal cysts-intellectual disability syndrome ()
........expandhirsutism-skeletal dysplasia-intellectual disability syndrome ()
........expandholoprosencephaly-radial heart renal anomalies syndrome ()
........expandinfantile choroidocerebral calcification syndrome ()
........expandisolated anencephaly/exencephaly ()
........expandJohnson neuroectodermal syndrome ()
........expandKBG syndrome ()
........expandLenz-Majewski hyperostotic dwarfism ()
........expandmicrocephaly-deafness-intellectual disability syndrome ()
........expandMoynahan syndrome ()
........expandMyhre syndrome ()
........expandomphalocele syndrome, Shprintzen-Goldberg type ()
........expandophthalmoplegia-intellectual disability-lingua scrotalis syndrome ()
........expandorofaciodigital syndrome V ()
........expandorofaciodigital syndrome X ()
........expandpolymicrogyria ()
........expandprolidase deficiency ()
........expandpseudoprogeria syndrome ()
........expandRamos-Arroyo syndrome ()
........expandShprintzen-Goldberg syndrome ()
........expandSmith-Magenis syndrome ()
........expandspastic paraplegia-epilepsy-intellectual disability syndrome ()
........expandspastic paraplegia-nephritis-deafness syndrome ()
........expandStimmler syndrome ()
........expandtemtamy syndrome ()
........expandtrichorhinophalangeal syndrome type II ()
........expanduveal coloboma-cleft lip and palate-intellectual disability ()
........expandWilliams syndrome ()
........expandWolf-Hirschhorn syndrome ()
........expandZimmermann-Laband syndrome ()



 Sister Nodes: 
..expandAchard syndrome ()
..expandAchenbach syndrome ()
..expandacute chest syndrome ()
..expandacute coronary syndrome ()
..expandadult respiratory distress syndrome ()
..expandanterior spinal artery syndrome ()
..expandantiphospholipid syndrome ()
..expandautosomal dominant chondrodysplasia punctata ()
..expandBarre-Lieou syndrome ()
..expandbrachydactyly-nystagmus-cerebellar ataxia syndrome ()
..expandBrown-Sequard syndrome ()
..expandburning mouth syndrome ()
..expandCADASIL ()
..expandCapgras syndrome ()
..expandcapillary leak syndrome ()
..expandcarcinoid syndrome ()
..expandcauda equina syndrome ()
..expandcentral sleep apnea syndrome ()
..expandcleidocranial dysplasia ()
..expandcompartment syndrome ()
..expanddiffuse infiltrative lymphocytosis syndrome ()
..expanddry eye syndrome ()
..expandDuane retraction syndrome ()
..expanddumping syndrome ()
..expandempty sella syndrome ()
..expandeuthyroid sick syndrome ()
..expandFanconi syndrome ()
..expandFG syndrome ()
..expandfibrogenesis imperfecta ossium ()
..expandfibromyalgia ()
..expandFroelich syndrome ()
..expandFuchs' heterochromic uveitis ()
..expandGorham disease ()
..expandhepatorenal syndrome ()
..expandhypoplastic left heart syndrome ()
..expandinclusion body myopathy with Paget disease of bone and frontotemporal dementia ()
..expandirritable bowel syndrome ()
..expandKluver-Bucy syndrome ()
..expandlateral medullary syndrome ()
..expandlong QT syndrome ()
..expandLown-Ganong-Levine syndrome ()
..expandmedian arcuate ligament syndrome ()
..expandmetabolic syndrome ()
..expandmiliaria ()
..expandmultiple chemical sensitivity ()
..expandmyalgic encephalomeyelitis/chronic fatigue syndrome ()
..expandnephrotic syndrome ()
..expandobstructive sleep apnea syndrome ()
..expandpalindromic rheumatism ()
..expandPatau syndrome ()
..expandpersian gulf syndrome ()
..expandPotter syndrome ()
..expandReye syndrome ()
..expandsick sinus syndrome ()
..expandsubclavian steal syndrome ()
..expandsubstance withdrawal syndrome ()
..expandsuperior mesenteric artery syndrome ()
..expandsyndromic intellectual disability ()
..expandtarsal tunnel syndrome ()
..expandtethered spinal cord syndrome ()
..expandthoracic outlet syndrome ()
..expandTietze syndrome ()
..expandtoxic shock syndrome ()
..expandvertebral artery insufficiency ()
..expandWaterhouse-Friderichsen syndrome ()
..expandWissler syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:508
Name:syndromic intellectual disability
Definition:A intellectual disability that is part of a larger syndrome.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:syndrome associated with intellectual disability; syndrome associated with intellectual disability; syndromic intellectual disability
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal