{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0019587/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"entity",
"hearing loss",
"hearing disorder",
"hereditary neurological disease",
"nervous system disease",
"sensory system disease",
"nonsyndromic genetic hearing loss",
"auditory system disease",
"auditory system disorder",
"autosomal genetic disease",
"perceptual disorders",
"genetic disorder",
"realizable",
"autosomal dominant disease",
"disposition",
"hereditary disease",
"continuant",
"inherited auditory system disease",
"characteristic",
"disease",
"experimental factor",
"hearing loss disorder",
"human disease",
"nervous system disorder",
"psychiatric disorder",
"autosomal dominant nonsyndromic hearing loss"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:57:32.301923+00:00",
"name": "MONDO_0019587",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:09:15.124879+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "autosomal dominant nonsyndromic hearing loss",
"synonyms": [
"autosomal dominant isolated sensorineural hearing loss type DFNA",
"autosomal dominant non-syndromic neurosensory hearing loss type DFNA",
"autosomal dominant isolated neurosensory hearing loss type DFNA",
"autosomal dominant nonsyndromic hearing loss",
"autosomal dominant non-syndromic sensorineural hearing loss type DFNA",
"autosomal dominant nonsyndromic hearing impairment"
],
"term_id": "MONDO:0019587",
"term_name": "autosomal dominant nonsyndromic hearing loss",
"uuid": "ec02dbab-dbfa-470e-9956-759dc21dc960"
}