MONDO:0010459

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0010459/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "aliases": [
        "kyle-gaulton:phenotype_amyotrophicLateralSclerosisType15"
    ],
    "ancestors": [
        "specifically dependent continuant",
        "hereditary motor neuron disease",
        "nervous system disorder",
        "experimental factor",
        "realizable entity",
        "genetic disorder",
        "central nervous system disease",
        "inherited neurodegenerative disorder",
        "entity",
        "motor neuron disorder",
        "neuromuscular disease",
        "neurodegenerative disease",
        "motor neuron disease",
        "anterior horn disorder",
        "spinal cord disorder",
        "disposition",
        "continuant",
        "spinal cord disease",
        "amyotrophic lateral sclerosis",
        "disease",
        "hereditary disease",
        "neuropathy",
        "familial amyotrophic lateral sclerosis",
        "human disease",
        "amyotrophic lateral sclerosis type 15",
        "nervous system disease",
        "central nervous system disorder"
    ],
    "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",
        "ALS15",
        "amyotrophic lateral sclerosis type 15",
        "UBQLN2 amyotrophic lateral sclerosis",
        "amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant",
        "amyotrophic lateral sclerosis caused by mutation in UBQLN2",
        "amyotrophic lateral sclerosis 15, with or without frontotemporal dementia"
    ],
    "term_id": "MONDO:0010459",
    "term_name": "amyotrophic lateral sclerosis type 15",
    "uuid": "ffac462a-1554-402c-9018-5e906e0f4cff"
}