MONDO:0008371

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0008371/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "ancestors": [
        "skin disorder",
        "inborn errors of metabolism",
        "experimental factor",
        "Dowling-Degos disease",
        "realizable",
        "skin disease",
        "disorder of fucoglycosan synthesis",
        "genetic disorder",
        "hyperpigmentation of the skin",
        "integumentary system disease",
        "integumentary system disorder",
        "reticulate pigment disorder",
        "disorder of protein O-glycosylation",
        "characteristic",
        "hereditary disease",
        "disorder of glycosylation",
        "human disease",
        "glycoprotein metabolism disease",
        "skin pigmentation disorder",
        "metabolic disease",
        "continuant",
        "disposition",
        "hereditary skin disorder",
        "disease",
        "congenital disorder of glycosylation",
        "entity"
    ],
    "audit": {},
    "creation_timestamp": "2023-11-03T21:56:08.139561+00:00",
    "name": "MONDO_0008371",
    "ontology": "MONDO",
    "release_timestamp": "2023-11-06T21:06:24.731794+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
        "title": "Ingrid Youngworth"
    },
    "summary": "Dowling-Degos disease",
    "synonyms": [
        "Dowling-Degos disease type 1",
        "dark dot disease",
        "reticular pigment anomaly of flexures"
    ],
    "term_id": "MONDO:0008371",
    "term_name": "Dowling-Degos disease",
    "uuid": "fd4d0d46-4fb3-4150-83de-02f0240b0ab9"
}