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

ONTOLOGY REPORT - ANNOTATIONS


Term:Fanconi anemia complementation group D1
go back to main search page
Accession:DOID:0111089 term browser browse the term
Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRCA2 gene on chromosome 13q13. (DO)
Synonyms:exact_synonym: FAD1;   FANCD1
 primary_id: MESH:C563980
 alt_id: OMIM:605724;   RDO:0013089
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
Fanconi anemia complementation group D1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Brca2 BRCA2, DNA repair associated JBrowse link 12 503,660 544,754 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15603
    Nutritional and Metabolic Diseases 4390
      disease of metabolism 4390
        DNA Repair-Deficiency Disorders 202
          Fanconi anemia 43
            Fanconi anemia complementation group D1 1
Path 2
Term Annotations click to browse term
  disease 15603
    disease of anatomical entity 14934
      Hemic and Lymphatic Diseases 1724
        hematopoietic system disease 1452
          bone marrow disease 403
            aplastic anemia 150
              congenital hypoplastic anemia 104
                Fanconi anemia 43
                  Fanconi anemia complementation group D1 1
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.