ONTOLOGY REPORT - ANNOTATIONS


Term:learning disability
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Accession:DOID:8927 term browser browse the term
Definition:Conditions characterized by a significant discrepancy between an individual's perceived level of intellect and their ability to acquire new language and other cognitive skills. These disorders may result from organic or psychological conditions. Relatively common subtypes include DYSLEXIA, DYSCALCULIA, and DYSGRAPHIA.
Synonyms:exact_synonym: Adult Learning Disorders;   Developmental Academic Disorder;   Developmental Academic Disorders;   Developmental Disorders of Scholastic Skills;   Learning Disabilities;   Learning Disorder;   Learning Disorders;   Learning Disturbance;   Learning Disturbances;   academic skill disorder;   adult learning disorder;   scholastic skills development disorders
 narrow_synonym: SPECIFIC LEARNING DISABILITY
 primary_id: MESH:D007859
 alt_id: RDO:0002319
For additional species annotation, visit the Alliance of Genome Resources.


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learning disability term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ache acetylcholinesterase JBrowse link 12 22,472,358 22,477,052 RGD:11554173
G Adar adenosine deaminase, RNA-specific JBrowse link 2 189,045,551 189,085,448 RGD:8554872
G Apod apolipoprotein D JBrowse link 11 72,705,204 72,726,263 RGD:11554173
G App amyloid beta precursor protein JBrowse link 11 24,425,013 24,641,872 RGD:11554173
G Bcl2 BCL2, apoptosis regulator JBrowse link 13 26,605,426 26,769,374 RGD:11554173
G Camkmt calmodulin-lysine N-methyltransferase JBrowse link 6 8,346,645 8,729,773 RGD:11554173
G Cntnap2 contactin associated protein-like 2 JBrowse link 4 74,700,539 77,025,463 RGD:13450914
G Dbn1 drebrin 1 JBrowse link 17 9,679,511 9,693,878 RGD:10398819
G Elavl4 ELAV like RNA binding protein 4 JBrowse link 5 130,001,387 130,144,557 RGD:9685325
G Ghr growth hormone receptor JBrowse link 2 53,149,225 53,413,954 RGD:11566045
G Gria1 glutamate ionotropic receptor AMPA type subunit 1 JBrowse link 10 42,441,723 42,760,200 RGD:11554173
G Hmox1 heme oxygenase 1 JBrowse link 19 14,508,634 14,515,455 RGD:11554173
G Htr1a 5-hydroxytryptamine receptor 1A JBrowse link 2 36,246,628 36,247,896 RGD:11554173
G Htr7 5-hydroxytryptamine receptor 7 JBrowse link 1 254,547,964 254,671,811 RGD:11554173
G Ikbkg inhibitor of nuclear factor kappa B kinase regulatory subunit gamma JBrowse link X 156,254,187 156,280,046 RGD:12791267
G Il1b interleukin 1 beta JBrowse link 3 121,876,256 121,882,637 RGD:11554173
G Il1rn interleukin 1 receptor antagonist JBrowse link 3 1,449,778 1,468,624 RGD:7175060
RGD:11554173
G Il6 interleukin 6 JBrowse link 4 3,043,231 3,047,807 RGD:7829733
G Iqsec2 IQ motif and Sec7 domain 2 JBrowse link X 22,212,137 22,293,810 RGD:8554872
G Kl Klotho JBrowse link 12 942,974 987,206 RGD:11554173
G Mapt microtubule-associated protein tau JBrowse link 10 92,289,002 92,386,517 RGD:11554173
G Mecp2 methyl CpG binding protein 2 JBrowse link X 156,650,389 156,713,813 RGD:11554173
G Micu1 mitochondrial calcium uptake 1 JBrowse link 20 29,284,833 29,433,617 RGD:11554173
G Mir124-3 microRNA 124-3 JBrowse link 3 176,406,205 176,406,291 RGD:11554173
G Mt1 metallothionein 1 JBrowse link 19 11,301,991 11,303,007 RGD:11554173
G Mt2A metallothionein 2A JBrowse link 19 11,307,966 11,308,740 RGD:11554173
G Nf1 neurofibromin 1 JBrowse link 10 66,732,460 66,928,706 RGD:1302541
RGD:11554173
G Ntf4 neurotrophin 4 JBrowse link 1 101,405,314 101,408,145 RGD:737722
G Pafah1b1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 JBrowse link 10 61,456,144 61,577,412 RGD:12790586
G Pde1b phosphodiesterase 1B JBrowse link 7 145,117,951 145,147,711 RGD:11554173
G Pnoc prepronociceptin JBrowse link 15 48,805,841 48,833,071 RGD:11554173
G Por cytochrome p450 oxidoreductase JBrowse link 12 23,998,411 24,017,063 RGD:11554173
G Prkn parkin RBR E3 ubiquitin protein ligase JBrowse link 1 48,880,015 50,069,998 RGD:11554173
G Psen1 presenilin 1 JBrowse link 6 107,169,514 107,221,000 RGD:11554173
G Rnf135 ring finger protein 135 JBrowse link 10 67,531,989 67,551,237 RGD:11554173
G Sigmar1 sigma non-opioid intracellular receptor 1 JBrowse link 5 58,121,824 58,124,687 RGD:11554173
G Slc17a6 solute carrier family 17 member 6 JBrowse link 1 106,980,463 107,038,717 RGD:11554173
G Slc17a7 solute carrier family 17 member 7 JBrowse link 1 101,161,265 101,172,292 RGD:11554173
G Syp synaptophysin JBrowse link X 15,694,699 15,709,244 RGD:11554173
G Th tyrosine hydroxylase JBrowse link 1 216,073,034 216,080,287 RGD:11554173
G Tlr4 toll-like receptor 4 JBrowse link 5 82,587,424 82,601,056 RGD:11554173
G Trh thyrotropin releasing hormone JBrowse link 4 124,110,716 124,113,242 RGD:11554173
G Vegfa vascular endothelial growth factor A JBrowse link 9 17,340,341 17,355,681 RGD:11554173
chromosome 17q11.2 deletion syndrome, 1.4Mb term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rnf135 ring finger protein 135 JBrowse link 10 67,531,989 67,551,237 RGD:8554872
dyslexia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dcdc2 doublecortin domain containing 2 JBrowse link 17 41,838,201 42,031,265 RGD:12910971
RGD:12910976
RGD:12910975
RGD:12910973
RGD:11532935
G Dnaaf4 dynein axonemal assembly factor 4 JBrowse link 8 79,637,678 79,651,892 RGD:7240710
RGD:8554872
G Drd4 dopamine receptor D4 JBrowse link 1 214,278,296 214,282,818 RGD:13209014
G Foxp2 forkhead box P2 JBrowse link 4 41,364,441 41,944,685 RGD:11535997
G Ncan neurocan JBrowse link 16 21,050,243 21,076,707 RGD:8554872
G RGD1307443 similar to mKIAA0319 protein JBrowse link 17 42,163,245 42,226,725 RGD:7240710
reading disorder term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cntnap2 contactin associated protein-like 2 JBrowse link 4 74,700,539 77,025,463 RGD:13450919
Riddle syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rnf168 ring finger protein 168 JBrowse link 11 71,721,242 71,743,421 RGD:7240710
RGD:8554872
Stormorken syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Stim1 stromal interaction molecule 1 JBrowse link 1 167,373,894 167,533,412 RGD:7240710
RGD:8554872
X-Linked Epilepsy, with Variable Learning Disabilities and Behavior Disorders term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Syn1 synapsin I JBrowse link X 1,321,315 1,379,202 RGD:7240710
RGD:8554872
G Timp1 TIMP metallopeptidase inhibitor 1 JBrowse link X 1,364,771 1,369,451 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14823
    Developmental Diseases 7637
      Neurodevelopmental Disorders 2755
        learning disability 74
          Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB 0
          Giacheti Syndrome 0
          Riddle syndrome 1
          Slavotinek Pike Mills Hurst Syndrome 0
          Specific Learning Disorder 0
          X-Linked Epilepsy, with Variable Learning Disabilities and Behavior Disorders 2
          chromosome 17q11.2 deletion syndrome, 1.4Mb 1
          distal 10q deletion syndrome 0
          dyscalculia 0
          dyslexia + 7
          reading disorder + 8
          writing disorder + 0
Path 2
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        central nervous system disease 6908
          brain disease 6412
            disease of mental health 4323
              developmental disorder of mental health 2594
                specific developmental disorder 1329
                  communication disorder 214
                    learning disability 74
                      Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB 0
                      Giacheti Syndrome 0
                      Riddle syndrome 1
                      Slavotinek Pike Mills Hurst Syndrome 0
                      Specific Learning Disorder 0
                      X-Linked Epilepsy, with Variable Learning Disabilities and Behavior Disorders 2
                      chromosome 17q11.2 deletion syndrome, 1.4Mb 1
                      distal 10q deletion syndrome 0
                      dyscalculia 0
                      dyslexia + 7
                      reading disorder + 8
                      writing disorder + 0
paths to the root

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