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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:Aggressive Fibromatosis
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Accession:DOID:9003291 term browser browse the term
Definition:A childhood counterpart of abdominal or extra-abdominal desmoid tumors, characterized by firm subcutaneous nodules that grow rapidly in any part of the body but do not metastasize. The adult form of abdominal fibromatosis is FIBROMATOSIS, ABDOMINAL. (Stedman, 25th ed)
Synonyms:exact_synonym: Aggressive Fibromatoses;   Desmoid;   Desmoids
 primary_id: MESH:D018222
 alt_id: RDO:0001321
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
 
Aggressive Fibromatosis term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Apc APC regulator of WNT signaling pathway ISO CTD Direct Evidence: marker/mechanism CTD PMID:11816139 NCBI chr18:27,011,710...27,106,323
Ensembl chr18:27,047,382...27,105,531
JBrowse link
G Ccn2 cellular communication network factor 2 ISO mRNA:increased expression:tumor (human) RGD PMID:19366727 RGD:2314525 NCBI chr 1:21,851,657...21,854,773
Ensembl chr 1:21,851,660...21,854,773
JBrowse link
G Serpine1 serpin family E member 1 susceptibility ISO associated with Adenomatous Polyposis Coli;DNA:polymorphism:promoter:rs1799768 (human) RGD PMID:17160433 RGD:13208596 NCBI chr12:22,641,104...22,651,482
Ensembl chr12:22,641,104...22,651,482
JBrowse link
G Tnf tumor necrosis factor ISO CTD Direct Evidence: therapeutic CTD PMID:19944662 NCBI chr20:5,189,382...5,192,000
Ensembl chr20:5,189,390...5,192,000
JBrowse link
hereditary desmoid disease term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Apc APC regulator of WNT signaling pathway ISO ClinVar Annotator: match by term: Desmoid disease, hereditary
ClinVar Annotator: match by OMIM:135290
OMIM
ClinVar
PMID:1316610, PMID:1324223, PMID:1338764, PMID:1944466, PMID:8162022, PMID:8187091, PMID:8381579, PMID:8381580, PMID:8844222, PMID:8940264, PMID:8990002, PMID:9342373, PMID:9664575, PMID:9950360, PMID:10077730, PMID:10083733, PMID:10094547, PMID:10470088, PMID:10713886, PMID:10768871, PMID:10782927, PMID:11748858, PMID:11933206, PMID:12007223, PMID:12034871, PMID:12173026, PMID:12357334, PMID:12901799, PMID:15024739, PMID:15108286, PMID:15108288, PMID:15300853, PMID:15459959, PMID:15857185, PMID:15951963, PMID:16088911, PMID:16134147, PMID:16292097, PMID:16317745, PMID:16461775, PMID:17411426, PMID:17489848, PMID:17785554, PMID:17963004, PMID:18199528, PMID:18433509, PMID:19029688, PMID:19444466, PMID:19531215, PMID:19793053, PMID:20223039, PMID:20301519, PMID:20649969, PMID:20685668, PMID:20924072, PMID:21110124, PMID:21859464, PMID:21901162, PMID:22431159, PMID:22703879, PMID:23159591, PMID:23970361, PMID:24033266, PMID:24123366, PMID:24448499, PMID:24573554, PMID:24599579, PMID:24728327, PMID:24735542, PMID:25186627, PMID:25203624, PMID:25479140, PMID:25525159, PMID:25590978, PMID:25637381, PMID:25741868, PMID:25801821, PMID:25925381, PMID:25980754, PMID:25992589, PMID:26138249, PMID:26300997, PMID:26320869, PMID:26446593, PMID:26467025, PMID:26493165, PMID:26580448, PMID:26613750, PMID:26681312, PMID:26845104, PMID:26976419, PMID:27150160, PMID:27153395, PMID:27600092, PMID:27878467, PMID:27978560, PMID:28135145, PMID:28492532, PMID:28608266, PMID:28873162, PMID:29641532, PMID:29684080, PMID:29915797, PMID:29945567, PMID:30374176, PMID:30613976, PMID:31428572 NCBI chr18:27,011,710...27,106,323
Ensembl chr18:27,047,382...27,105,531
JBrowse link
G Ctnnb1 catenin beta 1 ISO ClinVar Annotator: match by term: DESMOID TUMOR CAUSED BY SOMATIC MUTATION ClinVar PMID:9500465, PMID:9927029, PMID:10398436, PMID:10435629, PMID:10655994, PMID:26619011, PMID:26822237 NCBI chr 8:129,601,511...129,628,378
Ensembl chr 8:129,617,812...129,627,372
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16045
    disease of anatomical entity 15292
      musculoskeletal system disease 5737
        musculoskeletal system benign neoplasm 75
          connective tissue benign neoplasm 30
            fibroma 20
              Aggressive Fibromatosis 5
                hereditary desmoid disease 2
Path 2
Term Annotations click to browse term
  disease 16045
    disease of anatomical entity 15292
      nervous system disease 10879
        peripheral nervous system disease 2476
          neuropathy 2297
            neuromuscular disease 1778
              muscular disease 1201
                muscle tissue disease 813
                  Muscle Tissue Neoplasms 134
                    musculoskeletal system benign neoplasm 75
                      connective tissue benign neoplasm 30
                        fibroma 20
                          Aggressive Fibromatosis 5
                            hereditary desmoid disease 2
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.