Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia
go back to main search page
Accession:DOID:9003890 term browser browse the term
Synonyms:exact_synonym: Gata1-Related Cytopenia;   Gata1-Related X-Linked Cytopenia;   X-linked macrothrombocytopenia;   XLTDA
 narrow_synonym: GATA-1-RELATED THROMBOCYTOPENIA WITH DYSERYTHROPOIESIS;   THROMBOCYTOPENIA, X-LINKED, WITH DYSERYTHROPOIETIC ANEMIA;   THROMBOCYTOPENIA, X-LINKED, WITHOUT DYSERYTHROPOIETIC ANEMIA;   dyserythropoietic anemia and thrombocytopenia;   dyserythropoietic anemia with thrombocytopenia
 primary_id: MESH:C564525;   MESH:C564526
 alt_id: MIM:300367;   RDO:0008582;   RDO:0013462;   RDO:0013463


GViewer not supported for the selected species.

show annotations for term's descendants           Sort by:
X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gata1 GATA binding protein 1 ISO ClinVar Annotator: match by term: GATA1-Related X-Linked Cytopenia | ClinVar Annotator: match by term: Thrombocytopenia, X-linked, with or without dyserythropoietic anemia | ClinVar Annotator: match by term: Thrombocytopenia, X-linked, without dyserythropoietic anemia OMIM
ClinVar
PMID:871527 PMID:3164080 PMID:10700180 PMID:11418466 PMID:11809723 More... NCBI chrNW_004624893:595,948...602,980
Ensembl chrNW_004624893:595,967...602,979
JBrowse link
G Zrsr2 zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 ISO DNA:missense mutation:multiple (human) RGD PMID:28942350 RGD:151232291 NCBI chrNW_004624829:578,380...605,119
Ensembl chrNW_004624829:578,326...604,594
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14093
    physical disorder 4612
      congenital hemolytic anemia 294
        congenital dyserythropoietic anemia 23
          X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia 2
Path 2
Term Annotations click to browse term
  disease 14093
    disease of anatomical entity 13772
      Hemic and Lymphatic Diseases 3370
        hematopoietic system disease 2918
          anemia 679
            normocytic anemia 584
              hemolytic anemia 351
                congenital hemolytic anemia 294
                  congenital dyserythropoietic anemia 23
                    X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia 2
paths to the root