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aggressive fibromatosis English (Q475086)

Item Discussion
connective tissue benign neoplasm that occur most often in the abdomen, arms and legs English
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Language Label Description Also known as
British English
No label defined
No description defined

    Statements

    Freebase ID
    /m/0d6qjy
    1 reference
    stated in
    Q15241312 (Deleted Item)
    publication date
    28 October 2013
    Commons category
    Desmoid tumor
    0 references
    JSTOR topic ID
    aggressive-fibromatosis
    0 references
    MeSH
    D018222
    named as
    Fibromatosis, Aggressive
    1 reference
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0100245
    MeSH Code
    C04.557.450.565.590.340.410
    0 references
    health speciality
    Q162555 (Deleted Item)
    0 references
    Human Phenotype Ontology ID English
    HP:0100245
    1 reference
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0100245
    UMLS CUI English
    C0079218
    1 reference
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0100245
    MonDO ID
    MONDO:0019492
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0019492
    subclass of
    fibromatosis English
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0019492
    Q18553680 (Deleted Item)
    1 reference
    stated in
    Disease Ontology English
    retrieved
    30 November 2020
    Disease Ontology ID
    DOID:0080366
    Disease Ontology ID
    DOID:0080366
    1 reference
    stated in
    Disease Ontology English
    retrieved
    30 November 2020
    Disease Ontology ID
    DOID:0080366
    Genetics Home Reference Conditions ID English
    desmoid-tumor
    0 references
    Microsoft Academic ID
    2779677255
    0 references
    2910398736
    0 references
    ICD-O English
    8821/1
    0 references
    GARD rare disease ID
    1820
    0 references
    OpenAlex ID
    C2779677255
    1 reference
    stated in
    Q107507571 (Deleted Item)
    retrieved
    26 January 2022
    reference URL
    https://docs.openalex.org/download-snapshot/snapshot-data-format
    instance of
    Q112193867 (Deleted Item)
    0 references
     
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