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ONTOLOGY REPORT - ANNOTATIONS


Term:Specific Granule Deficiency
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Accession:DOID:9000265 term browser browse the term
Synonyms:exact_synonym: Lactoferrin-Deficient Neutrophils;   Neutrophil Lactoferrin Deficiency
 primary_id: MESH:C562873
 alt_id: RDO:0012406
 xref: OMIM:PS245480
For additional species annotation, visit the Alliance of Genome Resources.


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Specific Granule Deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cebpe CCAAT/enhancer binding protein epsilon JBrowse link 15 33,356,119 33,357,517 RGD:8554872
RGD:11554173
G Smarcd2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 JBrowse link 10 94,451,866 94,460,732 RGD:11554173
RGD:8554872
Specific Granule Deficiency 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cebpe CCAAT/enhancer binding protein epsilon JBrowse link 15 33,356,119 33,357,517 RGD:7240710
Specific Granule Deficiency 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Smarcd2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 JBrowse link 10 94,451,866 94,460,732 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15469
    disease of anatomical entity 14820
      hematopoietic system disease 1466
        leukocyte disease 471
          Specific Granule Deficiency 2
            Specific Granule Deficiency 1 1
            Specific Granule Deficiency 2 1
Path 2
Term Annotations click to browse term
  disease 15469
    disease of anatomical entity 14820
      Hemic and Lymphatic Diseases 1744
        hematopoietic system disease 1466
          leukocyte disease 471
            Specific Granule Deficiency 2
              Specific Granule Deficiency 1 1
              Specific Granule Deficiency 2 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.