ONTOLOGY REPORT - ANNOTATIONS


Term:Nestor-Guillermo Progeria Syndrome
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Accession:DOID:9000907 term browser browse the term
Synonyms:exact_synonym: NGPS;   PROGERIA SYNDROME, CHILDHOOD-ONSET, WITH OSTEOLYSIS;   PSCOO
 primary_id: OMIM:614008;   RDO:9000610
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Nestor-Guillermo Progeria Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Banf1 barrier to autointegration factor 1 JBrowse link 1 220,744,195 220,746,224 RGD:7240710
RGD:8554872
G Eif1ad eukaryotic translation initiation factor 1A domain containing JBrowse link 1 220,746,387 220,751,687 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14823
    syndrome 4218
      Nestor-Guillermo Progeria Syndrome 2
Path 2
Term Annotations click to browse term
  disease 14823
    Developmental Diseases 7637
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6675
        genetic disease 5920
          monogenic disease 2859
            autosomal genetic disease 2140
              autosomal recessive disease 1257
                progeria 15
                  Progeria Syndrome, Childhood-Onset 3
                    Nestor-Guillermo Progeria Syndrome 2
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.