MONDO:0012866

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0012866/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "ancestors": [
        "nervous system disorder",
        "neurodegenerative disease",
        "inherited neurodegenerative disorder",
        "entity",
        "hereditary disease",
        "hereditary neuromuscular disease",
        "experimental factor",
        "paraplegia",
        "central nervous system disease",
        "realizable",
        "human disease",
        "hereditary spastic paraplegia",
        "genetic disorder",
        "continuant",
        "palsy",
        "hereditary neurological disease",
        "neuropathy",
        "characteristic",
        "nervous system disease",
        "central nervous system disorder",
        "hereditary spastic paraplegia 35",
        "disposition",
        "neuromuscular disease",
        "disease"
    ],
    "audit": {},
    "creation_timestamp": "2023-11-03T21:59:25.901165+00:00",
    "name": "MONDO_0012866",
    "ontology": "MONDO",
    "release_timestamp": "2023-11-06T21:12:53.738289+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
        "title": "Ingrid Youngworth"
    },
    "summary": "hereditary spastic paraplegia 35",
    "synonyms": [
        "leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia",
        "FA2H hereditary spastic paraplegia",
        "autosomal recessive spastic paraplegia 35",
        "hereditary spastic paraplegia type 35",
        "hereditary spastic paraplegia 35",
        "autosomal recessive spastic paraplegia type 35",
        "hereditary spastic paraplegia caused by mutation in FA2H",
        "SPG35"
    ],
    "term_id": "MONDO:0012866",
    "term_name": "hereditary spastic paraplegia 35",
    "uuid": "e8b1f510-3824-4f8d-8355-c06c43e7ac43"
}