ONTOLOGY REPORT - ANNOTATIONS


Term:Microphthalmia, Syndromic 7
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Accession:DOID:9003200 term browser browse the term
Synonyms:exact_synonym: LSDMCA1;   Linear skin defects with multiple congenital anomalies 1;   MCOPS7;   MLS;   Microphthalmia with Linear Skin Defects Syndrome;   Microphthalmia with Linear Skin Lesions Syndrome;   Microphthalmia with linear skin defects;   Microphthalmia, dermal aplasia, and sclerocornea;   Midas Syndrome
 primary_id: MESH:C537466
 alt_id: OMIM:309801;   RDO:0003311
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Microphthalmia, Syndromic 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cox7b cytochrome c oxidase subunit 7B JBrowse link X 77,065,427 77,071,676 RGD:11554173
G Hccs holocytochrome c synthase JBrowse link X 26,294,028 26,303,461 RGD:7240710
RGD:8554872
G Ndufb11 NADH:ubiquinone oxidoreductase subunit B11 JBrowse link X 1,787,266 1,789,524 RGD:11554173
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    sensory system disease 4246
      eye and adnexa disease 1985
        eye disease 1985
          microphthalmia 89
            Microphthalmia, Syndromic 7 3
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        sensory system disease 4246
          eye and adnexa disease 1985
            eye disease 1985
              Eye Abnormalities 283
                microphthalmia 89
                  Microphthalmia, Syndromic 7 3
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.