MONDO:0013866

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0013866/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "entity",
11        "adult neuronal ceroid lipofuscinosis",
12        "genetic disorder",
13        "neuronal ceroid lipofuscinosis",
14        "central nervous system disease",
15        "psychiatric disorder",
16        "inherited neurodegenerative disorder",
17        "lysosomal lipid storage disorder",
18        "dementia",
19        "inherited lipid metabolism disorder",
20        "hereditary neurological disease",
21        "hereditary disease",
22        "continuant",
23        "realizable",
24        "disease",
25        "inborn errors of metabolism",
26        "lysosomal storage disease",
27        "nervous system disorder",
28        "metabolic disease",
29        "characteristic",
30        "brain disease",
31        "central nervous system disorder",
32        "neurodegenerative disease",
33        "experimental factor",
34        "cerebral lipidosis with dementia",
35        "mental or behavioural disorder",
36        "neuronal ceroid lipofuscinosis 11",
37        "nervous system disease",
38        "disposition",
39        "human disease",
40        "hereditary dementia",
41        "cognitive disorder",
42        "brain disorder"
43    ],
44    "audit": {},
45    "comments": [],
46    "creation_timestamp": "2023-11-03T21:50:12.033392+00:00",
47    "definition": "Any neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the GRN gene.",
48    "name": "MONDO_0013866",
49    "ontology": "MONDO",
50    "release_timestamp": "2023-11-06T21:33:09.661706+00:00",
51    "schema_version": "5",
52    "status": "released",
53    "submitted_by": {
54        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
55        "title": "Ingrid Youngworth"
56    },
57    "summary": "neuronal ceroid lipofuscinosis 11",
58    "synonyms": [
59        "neuronal ceroid lipofuscinosis caused by mutation in Grn",
60        "ceroid lipofuscinosis, neuronal, type 11",
61        "CLN11",
62        "neuronal ceroid lipofuscinosis caused by mutation in GRN",
63        "Grn neuronal ceroid lipofuscinosis",
64        "GRN neuronal ceroid lipofuscinosis",
65        "neuronal ceroid lipofuscinosis type 11"
66    ],
67    "term_id": "MONDO:0013866",
68    "term_name": "neuronal ceroid lipofuscinosis 11",
69    "uuid": "fc2760c5-1fc9-457c-9d5c-1f47699435d6"
70}