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


RGD uses the Human Disease Ontology (DO, 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:Fanconi anemia complementation group E
go back to main search page
Accession:DOID:0111084 term browser browse the term
Definition:A Fanconi anemia that has_material_basis_in homozygous mutation in the FANCE gene on chromosome 6p22-p21. (DO)
Synonyms:exact_synonym: FACE;   FANCE
 primary_id: OMIM:600901
 alt_id: RDO:0015797
 xref: NCI:C125709
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
Fanconi anemia complementation group E term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Fance FA complementation group E ISO ClinVar Annotator: match by OMIM:600901
ClinVar Annotator: match by term: Fanconi anemia, complementation group E
PMID:7662964, PMID:9382107, PMID:10205272, PMID:11001585, PMID:14695169, PMID:15609317, PMID:16774934, PMID:17308347, PMID:17924555, PMID:18271933, PMID:21279724, PMID:22778927, PMID:24033266, PMID:24728327, PMID:25058500, PMID:25741868, PMID:26822949, PMID:27165003, PMID:28492532, PMID:28678401, PMID:30311386, PMID:30609409 NCBI chr20:7,888,927...7,906,142
Ensembl chr20:7,895,083...7,906,142
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16108
    Nutritional and Metabolic Diseases 4720
      disease of metabolism 4720
        DNA Repair-Deficiency Disorders 258
          Fanconi anemia 43
            Fanconi anemia complementation group E 1
Path 2
Term Annotations click to browse term
  disease 16108
    disease of anatomical entity 15356
      Hemic and Lymphatic Diseases 2047
        hematopoietic system disease 1643
          bone marrow disease 473
            Bone Marrow Failure Disorders 162
              aplastic anemia 150
                congenital hypoplastic anemia 107
                  Fanconi anemia 43
                    Fanconi anemia complementation group E 1
paths to the root


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