MONDO:0030535

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0030535/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "epidermolysis bullosa simplex",
11        "skin disorder",
12        "continuant",
13        "disease",
14        "disposition",
15        "epidermolysis bullosa",
16        "integumentary system disease",
17        "experimental factor",
18        "hereditary disease",
19        "realizable",
20        "inherited epidermolysis bullosa",
21        "epidermal disease",
22        "genetic disorder",
23        "vesiculobullous skin disease",
24        "skin disease",
25        "entity",
26        "hereditary skin disorder",
27        "epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive",
28        "integumentary system disorder",
29        "human disease",
30        "characteristic"
31    ],
32    "audit": {},
33    "creation_timestamp": "2023-11-03T21:56:15.693196+00:00",
34    "name": "MONDO_0030535",
35    "ontology": "MONDO",
36    "release_timestamp": "2023-11-06T21:06:39.294278+00:00",
37    "schema_version": "4",
38    "status": "released",
39    "submitted_by": {
40        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
41        "title": "Ingrid Youngworth"
42    },
43    "summary": "epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive",
44    "synonyms": [
45        "EBS2D"
46    ],
47    "term_id": "MONDO:0030535",
48    "term_name": "epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive",
49    "uuid": "ebbd1adc-d5da-45df-9fd9-7fc7b49d4d5b"
50}