ONTOLOGY REPORT - ANNOTATIONS


Term:dyslexia
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Accession:DOID:4428 term browser browse the term
Definition:A cognitive disorder characterized by an impaired ability to comprehend written and printed words or phrases despite intact vision. This condition may be developmental or acquired. Developmental dyslexia is marked by reading achievement that falls substantially below that expected given the individual's chronological age, measured intelligence, and age-appropriate education. The disturbance in reading significantly interferes with academic achievement or with activities of daily living that require reading skills. (From DSM-IV)
Synonyms:exact_synonym: DYSLEXIA, SUSCEPTIBILITY TO, 1;   DYSLEXIA, SUSCEPTIBILITY TO, 2;   DYSLEXIA, SUSCEPTIBILITY TO, 3;   DYSLEXIA, SUSCEPTIBILITY TO, 5;   DYSLEXIA, SUSCEPTIBILITY TO, 6;   DYSLEXIA, SUSCEPTIBILITY TO, 8;   DYSLEXIA, SUSCEPTIBILITY TO, 9;   DYX1;   DYX2;   DYX3;   DYX5;   DYX6;   DYX8;   DYX9;   Developmental Dyslexia;   Developmental Dyslexias;   Developmental Reading Disabilities;   Developmental Reading Disability;   Developmental Reading Disorder;   Developmental Reading Disorders;   Dyslexias;   READING DISABILITY, SPECIFIC, 2;   Reading Disorder;   Reading Disorders;   WORD-BLINDNESS, CONGENITAL;   Word Blindness;   Word Blindnesses
 narrow_synonym: DYSLEXIA, SUSCEPTIBILITY TO, 7;   DYX4;   DYX7;   READING DISABILITY, SPECIFIC, 1 DYSLEXIA, SUSCEPTIBILITY TO, 4
 primary_id: MESH:D004410;   RDO:0005409
 alt_id: OMIM:127700;   OMIM:300509;   OMIM:600202;   OMIM:604254;   OMIM:606616;   OMIM:606896;   OMIM:608995
For additional species annotation, visit the Alliance of Genome Resources.


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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:8554872
RGD:11554173
RGD:7240710
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
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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14920
    Developmental Diseases 7769
      Neurodevelopmental Disorders 2765
        learning disability 74
          dyslexia 7
            Stormorken syndrome 1
            alexia + 0
Path 2
Term Annotations click to browse term
  disease 14920
    disease of anatomical entity 14086
      nervous system disease 9150
        central nervous system disease 6948
          brain disease 6454
            disease of mental health 4346
              developmental disorder of mental health 2600
                specific developmental disorder 1765
                  communication disorder 216
                    learning disability 74
                      reading disorder 8
                        dyslexia 7
                          Stormorken syndrome 1
                          alexia + 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.