{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0001516/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"motor neuron disease",
"nervous system disorder",
"nervous system disease",
"hereditary motor neuron disease",
"disease",
"genetic disorder",
"hereditary disease",
"continuant",
"spinal cord disorder",
"central nervous system disease",
"inherited neurodegenerative disorder",
"neurodegenerative disease",
"neuromuscular disease",
"neuropathy",
"spinal muscular atrophy",
"hereditary neurological disease",
"motor neuron disorder",
"central nervous system disorder",
"anterior horn disorder",
"human disease",
"disposition",
"entity",
"hereditary neuromuscular disease",
"spinal cord disease",
"realizable",
"experimental factor",
"characteristic"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:57:38.725482+00:00",
"name": "MONDO_0001516",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:09:29.151882+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "spinal muscular atrophy",
"synonyms": [],
"term_id": "MONDO:0001516",
"term_name": "spinal muscular atrophy",
"uuid": "f6296166-0e27-4223-b49d-e46252c05042"
}