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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:familial adenomatous polyposis 2
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Accession:DOID:0080410 term browser browse the term
Definition:A familial adenomatous polyposis that has_material_basis_in homozygous or compound heterozygous mutation in the MUTYH gene on chromosome 1p34. (DO)
Synonyms:exact_synonym: Adenomas, Multiple Colorectal, Autosomal Recessive;   Colorectal Adenomatous Polyposis, Autosomal Recessive;   FAP2;   MUTYH-related attenuated FAP;   MUTYH-related attenuated familial adenomatous polyposis;   MUTYH-related attenuated familial polyposis coli
 primary_id: MESH:C563924
 alt_id: OMIM:608456
 xref: ICD10CM:D12.6;   ORDO:247798
For additional species annotation, visit the Alliance of Genome Resources.

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16108
    syndrome 6992
      Hereditary Neoplastic Syndromes 815
        familial adenomatous polyposis 38
          familial adenomatous polyposis 2 1
Path 2
Term Annotations click to browse term
  disease 16108
    disease of anatomical entity 15356
      gastrointestinal system disease 4673
        Digestive System Neoplasms 1908
          Gastrointestinal Neoplasms 1768
            Intestinal Neoplasms 690
              Colorectal Neoplasms 669
                familial adenomatous polyposis 38
                  familial adenomatous polyposis 2 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.