Stockhub

scalp–ear–nipple syndrome English (Q7429841)

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

    Statements

    OMIM
    181270
    mapping relation type English
    exact match English
    2 references
    imported from Wikimedia project
    English Wikipedia
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    instance of
    malformation syndrome English
    0 references
    Q55788864 (Deleted Item)
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    Q929833 (Deleted Item)
    0 references
    disease
    1 reference
    stated in
    Q34714964 (Deleted Item)
    Q112193867 (Deleted Item)
    0 references
    Orphanet ID
    2036
    mapping relation type English
    exact match English
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    MeSH
    C536623
    mapping relation type English
    exact match English
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    subclass of
    ectodermal dysplasia English
    1 reference
    stated in
    Disease Ontology English
    retrieved
    27 November 2020
    Disease Ontology ID
    DOID:0111550
    Q55785290 (Deleted Item)
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    Q55785775 (Deleted Item)
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    Q55785863 (Deleted Item)
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    Q55788599 (Deleted Item)
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    Q18553439 (Deleted Item)
    1 reference
    stated in
    Disease Ontology English
    retrieved
    27 November 2020
    Disease Ontology ID
    DOID:0111550
    GARD rare disease ID
    159
    0 references
    BabelNet ID
    01903465n
    1 reference
    stated in
    BabelNet
    ICD-10-CM English
    Q87.8
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    MonDO ID
    MONDO:0008404
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    UMLS CUI English
    C1867020
    mapping relation type English
    exact match English
    1 reference
    stated in
    Q55345445 (Deleted Item)
    retrieved
    28 July 2018
    MonDO ID
    MONDO:0008404
    genetic association English
    Q18054278 (Deleted Item)
    2 references
    stated in
    Q905695 (Deleted Item)
    UniProt protein ID
    Q719H9
    retrieved
    13 August 2019
    stated in
    Q30448494 (Deleted Item)
    Microsoft Academic ID
    2776127363
    0 references
    ICD-11 (foundation) English
    88843032
    0 references
    Disease Ontology ID
    DOID:0111550
    1 reference
    stated in
    Disease Ontology English
    retrieved
    27 November 2020
    Disease Ontology ID
    DOID:0111550
     
    Retrieved from ‘https://stockhub.co/index.php?title=Item:Q7429841&oldid=5424642’