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thyroid dysgenesis English (Q7799746)

Item Discussion
human disease English
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Language Label Description Also known as
British English
No label defined
No description defined

    Statements

    MeSH
    D050033
    mapping relation type English
    Q39893184 (Deleted Item)
    named as
    Thyroid Dysgenesis
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    4 August 2018
    MonDO ID
    MONDO:0006666
    NCI Thesaurus ID English
    C26942
    1 reference
    stated in
    Disease Ontology English
    retrieved
    30 April 2015
    C26942
    mapping relation type English
    exact match English
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    4 August 2018
    MonDO ID
    MONDO:0006666
    GARD rare disease ID
    8426
    0 references
    MeSH Code
    C16.131.894
    0 references
    C19.874.689
    0 references
    ICD-9-CM
    246.8
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    4 August 2018
    MonDO ID
    MONDO:0006666
    MonDO ID
    MONDO:0006666
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    4 August 2018
    MonDO ID
    MONDO:0006666
    ICD-10-CM English
    E03.4
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    4 August 2018
    MonDO ID
    MONDO:0006666
    UMLS CUI English
    C0151516
    mapping relation type English
    Q39893184 (Deleted Item)
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    4 August 2018
    MonDO ID
    MONDO:0006666
    C0151516
    1 reference
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0005990
    C1563716
    1 reference
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0008188
    Disease Ontology ID
    DOID:2853
    mapping relation type English
    Q39893184 (Deleted Item)
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    4 August 2018
    MonDO ID
    MONDO:0006666
    DOID:2853
    1 reference
    stated in
    Disease Ontology English
    retrieved
    30 November 2020
    Disease Ontology ID
    DOID:2853
    Human Phenotype Ontology ID English
    HP:0005990
    1 reference
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0005990
    HP:0008188
    1 reference
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0008188
    health speciality
    Q162606 (Deleted Item)
    1 reference
    inferred from
    Q199897 (Deleted Item)
    Commons category
    Thyroid dysgenesis
    0 references
    Microsoft Academic ID
    2780648382
    0 references
    2911047824
    0 references
     
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