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ONTOLOGY REPORT - ANNOTATIONS


Term:Osteolysis Hereditary Multicentric
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Accession:DOID:9006569 term browser browse the term
Synonyms:exact_synonym: Al-Aqeel Sewairi Syndrome;   MONA;   MULTICENTRIC OSTEOLYSIS-NODULOSIS-ARTHROPATHY (MONA) SPECTRUM DISORDERS;   Multicentric Osteolysis, Nodulosis, and Arthropathy;   NAO SYNDROME;   Nodulosis-Arthropathy-Osteolysis Syndrome;   Torg Syndrome;   Torg osteolysis syndrome;   Torg-Winchester Syndrome
 primary_id: MESH:C536051;   RDO:0001465
 alt_id: OMIM:259600
For additional species annotation, visit the Alliance of Genome Resources.


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Osteolysis Hereditary Multicentric term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LPCAT2 lysophosphatidylcholine acyltransferase 2 JBrowse link 16 55,509,055 55,586,666 RGD:8554872
G MMP2 matrix metallopeptidase 2 JBrowse link 16 55,478,830 55,506,691 RGD:8554872
RGD:7240710
multicentric carpotarsal osteolysis syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G MAFB MAF bZIP transcription factor B JBrowse link 20 40,685,848 40,689,236 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16650
    disease of anatomical entity 15631
      musculoskeletal system disease 5428
        bone disease 3405
          bone resorption disease 167
            Osteolysis 23
              Osteolysis Hereditary Multicentric 3
                multicentric carpotarsal osteolysis syndrome 1
Path 2
Term Annotations click to browse term
  disease 16650
    disease of anatomical entity 15631
      musculoskeletal system disease 5428
        connective tissue disease 3932
          bone disease 3405
            bone remodeling disease 242
              bone resorption disease 167
                Osteolysis 23
                  Osteolysis Hereditary Multicentric 3
                    multicentric carpotarsal osteolysis syndrome 1
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.