MONDO:0030535

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0030535/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "ancestors": [
        "epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive",
        "disease",
        "genetic disorder",
        "entity",
        "realizable",
        "vesiculobullous skin disease",
        "disposition",
        "integumentary system disease",
        "hereditary disease",
        "human disease",
        "inherited epidermolysis bullosa",
        "characteristic",
        "integumentary system disorder",
        "skin disorder",
        "epidermolysis bullosa",
        "experimental factor",
        "hereditary skin disorder",
        "epidermolysis bullosa simplex",
        "epidermal disease",
        "continuant",
        "skin disease"
    ],
    "audit": {},
    "creation_timestamp": "2023-11-03T21:56:15.693196+00:00",
    "name": "MONDO_0030535",
    "ontology": "MONDO",
    "release_timestamp": "2023-11-06T21:06:39.294278+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
        "title": "Ingrid Youngworth"
    },
    "summary": "epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive",
    "synonyms": [
        "EBS2D"
    ],
    "term_id": "MONDO:0030535",
    "term_name": "epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive",
    "uuid": "ebbd1adc-d5da-45df-9fd9-7fc7b49d4d5b"
}