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ONTOLOGY REPORT - ANNOTATIONS


Term:Microphthalmia, Syndromic 2
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Accession:DOID:9002226 term browser browse the term
Synonyms:exact_synonym: ANOP2;   Cataracts, microphthalmia, radiculomegaly and septal heart defects;   MAA2;   MCOPS2;   Marashi Gorlin syndrome;   OFCD Syndrome;   Oculo facio cardio dental syndrome;   Oculofaciocardiodental syndrome
 primary_id: MESH:C537465;   RDO:0003309
 alt_id: OMIM:300166
For additional species annotation, visit the Alliance of Genome Resources.


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Microphthalmia, Syndromic 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Bcor BCL6 co-repressor JBrowse link X 11,570,155 11,692,022 RGD:7240710
RGD:8554872
RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15553
    Developmental Diseases 8823
      congenital heart disease 872
        heart septal defect 173
          Microphthalmia, Syndromic 2 1
Path 2
Term Annotations click to browse term
  disease 15553
    disease of anatomical entity 14837
      nervous system disease 10167
        sensory system disease 4596
          eye and adnexa disease 2148
            eye disease 2148
              lens disease 194
                cataract 187
                  Microphthalmia, Syndromic 2 1
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.