MONDO:0010459

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0010459/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "aliases": [
        "kyle-gaulton:phenotype_amyotrophicLateralSclerosisType15"
    ],
    "ancestors": [
        "nervous system disorder",
        "experimental factor",
        "central nervous system disease",
        "disposition",
        "disease",
        "motor neuron disorder",
        "genetic disorder",
        "inherited neurodegenerative disorder",
        "anterior horn disorder",
        "motor neuron disease",
        "neurodegenerative disease",
        "spinal cord disorder",
        "spinal cord disease",
        "hereditary motor neuron disease",
        "human disease",
        "central nervous system disorder",
        "entity",
        "realizable entity",
        "nervous system disease",
        "neuromuscular disease",
        "amyotrophic lateral sclerosis",
        "hereditary disease",
        "specifically dependent continuant",
        "amyotrophic lateral sclerosis type 15",
        "continuant",
        "familial amyotrophic lateral sclerosis",
        "neuropathy"
    ],
    "audit": {},
    "creation_timestamp": "2024-12-03T17:48:01.720471+00:00",
    "description": "amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant,amyotrophic lateral sclerosis caused by mutation in UBQLN2,ALS15,amyotrophic lateral sclerosis 15, with or without frontotemporal dementia,UBQLN2 amyotrophic lateral sclerosis,amyotrophic lateral sclerosis 15,amyotrophic lateral sclerosis type 15",
    "name": "MONDO_0010459",
    "ontology": "MONDO",
    "release_timestamp": "2025-01-10T04:16:55.164360+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/5e3038c4-baa5-4589-b3d8-ad2fe634e826/",
        "title": "Ying Sun"
    },
    "submitter_comment": "MONDO term",
    "summary": "amyotrophic lateral sclerosis type 15",
    "synonyms": [
        "amyotrophic lateral sclerosis 15, with or without frontotemporal dementia",
        "amyotrophic lateral sclerosis 15",
        "amyotrophic lateral sclerosis caused by mutation in UBQLN2",
        "UBQLN2 amyotrophic lateral sclerosis",
        "amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant",
        "amyotrophic lateral sclerosis type 15",
        "ALS15"
    ],
    "term_id": "MONDO:0010459",
    "term_name": "amyotrophic lateral sclerosis type 15",
    "uuid": "ffac462a-1554-402c-9018-5e906e0f4cff"
}