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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;   FLPIS;   Scott Bryant Graham Syndrome;   Scott craniodigital syndrome with mental retardation;   craniodigital syndrome-mental retardation, Scott type;   syndactyly type I with microcephaly and mental retardation
 primary_id: MESH:C538152
 alt_id: MESH:C537528;   OMIM:272440
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 16021
    syndrome 6144
      Filippi Syndrome 1
Path 2
Term Annotations click to browse term
  disease 16021
    Developmental Diseases 9337
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8165
        genetic disease 7689
          monogenic disease 5447
            autosomal genetic disease 4411
              autosomal dominant disease 2754
                complex cortical dysplasia with other brain malformations 528
                  Malformations of Cortical Development, Group I 378
                    microcephaly 222
                      Filippi Syndrome 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.