MONDO:0008009

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0008009/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "ancestors": [
        "realizable",
        "experimental factor",
        "human disease",
        "characteristic",
        "integumentary system disease",
        "entity",
        "disease",
        "autosomal dominant disease",
        "skin disease",
        "autosomal genetic disease",
        "monilethrix",
        "integumentary system disorder",
        "genetic disorder",
        "skin disorder",
        "hereditary disease",
        "hereditary skin disorder",
        "continuant",
        "disposition"
    ],
    "audit": {},
    "creation_timestamp": "2023-11-03T21:56:22.827535+00:00",
    "name": "MONDO_0008009",
    "ontology": "MONDO",
    "release_timestamp": "2023-11-06T21:06:53.190941+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
        "title": "Ingrid Youngworth"
    },
    "summary": "monilethrix",
    "synonyms": [
        "monilethrix",
        "moniliform hair syndrome"
    ],
    "term_id": "MONDO:0008009",
    "term_name": "monilethrix",
    "uuid": "f6423123-7d82-4d20-a857-aacb2d4aff4c"
}