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ONTOLOGY REPORT - ANNOTATIONS


Term:Lissencephaly 4
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Accession:DOID:9008921 term browser browse the term
Synonyms:exact_synonym: LIS4;   Lissencephaly 4, with Microcephaly
 primary_id: OMIM:614019;   RDO:9000520
For additional species annotation, visit the Alliance of Genome Resources.


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Lissencephaly 4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mir484 microRNA 484 JBrowse link 10 27,845 27,921 RGD:8554872
G Myh11 myosin heavy chain 11 JBrowse link 10 764,421 859,184 RGD:8554872
G Nde1 nudE neurodevelopment protein 1 JBrowse link 10 860,513 904,624 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16022
    physical disorder 764
      congenital nervous system abnormality 328
        lissencephaly 59
          Lissencephaly 4 3
Path 2
Term Annotations click to browse term
  disease 16022
    Developmental Diseases 9336
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8164
        genetic disease 7688
          monogenic disease 5446
            autosomal genetic disease 4409
              autosomal dominant disease 2753
                complex cortical dysplasia with other brain malformations 527
                  Malformations of Cortical Development, Group I 377
                    microcephaly 221
                      Lissencephaly 4 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.