MONDO:0010713

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0010713/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "ancestors": [
        "properdin deficiency, X-linked",
        "inborn error of immunity",
        "immune system disease",
        "experimental factor",
        "immune system disorder",
        "genetic disorder",
        "human disease",
        "continuant",
        "realizable",
        "immune deficiency disease",
        "disease",
        "hereditary disease",
        "entity",
        "disposition",
        "characteristic"
    ],
    "audit": {},
    "creation_timestamp": "2023-11-03T21:56:46.488193+00:00",
    "name": "MONDO_0010713",
    "ontology": "MONDO",
    "release_timestamp": "2023-11-06T21:07:38.529687+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
        "title": "Ingrid Youngworth"
    },
    "summary": "properdin deficiency, X-linked",
    "synonyms": [
        "properdin deficiency, X-linked, X-linked recessive",
        "properdin deficiency, X-linked"
    ],
    "term_id": "MONDO:0010713",
    "term_name": "properdin deficiency, X-linked",
    "uuid": "f2b02b30-5f2d-41e6-84cb-c5a2df2b2440"
}