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Schnyder corneal dystrophy English (Q4162393)

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

    Statements

    OMIM
    121800
    1 reference
    stated in
    Disease Ontology English
    retrieved
    28 August 2019
    Disease Ontology ID
    DOID:0060456
    subclass of
    Q21154082 (Deleted Item)
    2 references
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0007374
    stated in
    Disease Ontology English
    retrieved
    27 November 2020
    Disease Ontology ID
    DOID:0060456
    Q18553439 (Deleted Item)
    1 reference
    stated in
    Disease Ontology English
    retrieved
    27 November 2020
    Disease Ontology ID
    DOID:0060456
    Disease Ontology ID
    DOID:0060456
    1 reference
    stated in
    Disease Ontology English
    retrieved
    27 November 2020
    Disease Ontology ID
    DOID:0060456
    Commons category
    Schnyder crystalline corneal dystrophy
    0 references
    instance of
    Q929833 (Deleted Item)
    0 references
    Q112193867 (Deleted Item)
    0 references
    UMLS CUI English
    C0271287
    2 references
    stated in
    Disease Ontology English
    retrieved
    28 August 2019
    Disease Ontology ID
    DOID:0060456
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0007760
    Orphanet ID
    98967
    1 reference
    stated in
    Disease Ontology English
    retrieved
    28 August 2019
    Disease Ontology ID
    DOID:0060456
    GARD rare disease ID
    9277
    1 reference
    stated in
    Disease Ontology English
    retrieved
    28 August 2019
    Disease Ontology ID
    DOID:0060456
    MeSH
    C535475
    mapping relation type English
    exact match English
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0007374
    C535475
    2 references
    stated in
    Disease Ontology English
    retrieved
    28 August 2019
    Disease Ontology ID
    DOID:0060456
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0007760
    ICD-10-CM English
    H18.5
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0007374
    MonDO ID
    MONDO:0007374
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0007374
    Human Phenotype Ontology ID English
    HP:0007760
    1 reference
    stated in
    Q57084043 (Deleted Item)
    retrieved
    8 October 2018
    Human Phenotype Ontology ID English
    HP:0007760
    genetic association English
    Q18039691 (Deleted Item)
    2 references
    stated in
    Q905695 (Deleted Item)
    UniProt protein ID
    Q9Y5Z9
    retrieved
    13 August 2019
    stated in
    Q21092244 (Deleted Item)
    Microsoft Academic ID
    2781319546
    0 references
    KEGG ID English
    H00959
    0 references
    ICD-11 (foundation) English
    437801959
    0 references
     
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