MONDO:0001516

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0001516/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "spinal cord disease",
11        "spinal cord disorder",
12        "motor neuron disorder",
13        "hereditary neurological disease",
14        "experimental factor",
15        "hereditary disease",
16        "spinal muscular atrophy",
17        "inherited neurodegenerative disorder",
18        "anterior horn disorder",
19        "motor neuron disease",
20        "entity",
21        "continuant",
22        "realizable",
23        "human disease",
24        "neurodegenerative disease",
25        "central nervous system disease",
26        "hereditary neuromuscular disease",
27        "neuromuscular disease",
28        "nervous system disorder",
29        "neuropathy",
30        "nervous system disease",
31        "hereditary motor neuron disease",
32        "central nervous system disorder",
33        "disease",
34        "genetic disorder",
35        "disposition",
36        "characteristic"
37    ],
38    "audit": {},
39    "creation_timestamp": "2023-11-03T21:57:38.725482+00:00",
40    "name": "MONDO_0001516",
41    "ontology": "MONDO",
42    "release_timestamp": "2023-11-06T21:09:29.151882+00:00",
43    "schema_version": "4",
44    "status": "released",
45    "submitted_by": {
46        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
47        "title": "Ingrid Youngworth"
48    },
49    "summary": "spinal muscular atrophy",
50    "synonyms": [],
51    "term_id": "MONDO:0001516",
52    "term_name": "spinal muscular atrophy",
53    "uuid": "f6296166-0e27-4223-b49d-e46252c05042"
54}