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ONTOLOGY REPORT - ANNOTATIONS


Term:Filippi Syndrome
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Accession:DOID:9004403 term browser browse the term
Synonyms:exact_synonym: Craniodigital syndrome with mental retardation;   Craniodigital syndrome-mental retardation, Scott type;   FLPIS;   Scott Bryant Graham Syndrome;   Scott craniodigital syndrome with mental retardation;   Syndactyly type I with microcephaly and mental retardation
 primary_id: MESH:C538152
 alt_id: DOID:9008565;   MESH:C537528;   OMIM:272440;   RDO:0003386;   RDO:0004088
For additional species annotation, visit the Alliance of Genome Resources.


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Filippi Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ckap2l cytoskeleton associated protein 2-like JBrowse link 3 121,796,221 121,822,352 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15590
    syndrome 5131
      Filippi Syndrome 1
Path 2
Term Annotations click to browse term
  disease 15590
    Developmental Diseases 8723
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7503
        genetic disease 6993
          monogenic disease 4551
            autosomal genetic disease 3501
              autosomal dominant disease 2065
                complex cortical dysplasia with other brain malformations 477
                  Malformations of Cortical Development, Group I 334
                    microcephaly 206
                      Filippi Syndrome 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.