{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0010459/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"amyotrophic lateral sclerosis type 15",
"nervous system disorder",
"experimental factor",
"hereditary motor neuron disease",
"realizable",
"genetic disorder",
"inherited neurodegenerative disorder",
"spinal cord disease",
"hereditary neuromuscular disease",
"motor neuron disease",
"neuropathy",
"characteristic",
"hereditary disease",
"familial amyotrophic lateral sclerosis",
"central nervous system disorder",
"motor neuron disorder",
"human disease",
"nervous system disease",
"amyotrophic lateral sclerosis",
"anterior horn disorder",
"neuromuscular disease",
"hereditary neurological disease",
"continuant",
"disposition",
"disease",
"neurodegenerative disease",
"spinal cord disorder",
"central nervous system disease",
"entity"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:59:05.106626+00:00",
"name": "MONDO_0010459",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:12:10.752358+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "amyotrophic lateral sclerosis type 15",
"synonyms": [
"amyotrophic lateral sclerosis caused by mutation in UBQLN2",
"ALS15",
"amyotrophic lateral sclerosis 15, with or without frontotemporal dementia",
"amyotrophic lateral sclerosis type 15",
"UBQLN2 amyotrophic lateral sclerosis",
"amyotrophic lateral sclerosis 15",
"amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant"
],
"term_id": "MONDO:0010459",
"term_name": "amyotrophic lateral sclerosis type 15",
"uuid": "f65639ce-eca6-4125-8b4e-132c766c3b71"
}