MONDO:0007550

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0007550/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "ancestors": [
        "human disease",
        "hereditary skin disorder",
        "vesiculobullous skin disease",
        "realizable",
        "inherited epidermolysis bullosa",
        "epidermolysis bullosa",
        "experimental factor",
        "skin disease",
        "continuant",
        "integumentary system disorder",
        "epidermal disease",
        "entity",
        "integumentary system disease",
        "hereditary disease",
        "epidermolysis bullosa simplex 1A, generalized severe",
        "genetic disorder",
        "characteristic",
        "disposition",
        "disease",
        "skin disorder",
        "epidermolysis bullosa simplex"
    ],
    "audit": {},
    "creation_timestamp": "2023-11-03T21:56:06.693121+00:00",
    "name": "MONDO_0007550",
    "ontology": "MONDO",
    "release_timestamp": "2023-11-06T21:06:21.582925+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
        "title": "Ingrid Youngworth"
    },
    "summary": "epidermolysis bullosa simplex 1A, generalized severe",
    "synonyms": [
        "EBS, generalised severe",
        "EBS-gen sev",
        "epidermolysis bullosa simplex Dowling-Meara type",
        "generalised severe epidermolysis bullosa simplex",
        "epidermolysis bullosa simplex, herpetiformis",
        "EBS, generalized severe",
        "generalized severe epidermolysis bullosa simplex",
        "epidermolysis bullosa simplex 1A, generalized severe",
        "epidermolysis bullosa herpetiformis Dowling-Meara type",
        "EBSDM"
    ],
    "term_id": "MONDO:0007550",
    "term_name": "epidermolysis bullosa simplex 1A, generalized severe",
    "uuid": "eab91a8c-8ed8-40c7-b4a5-fc0f4548c516"
}