{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0019587/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"human disease",
"nonsyndromic genetic hearing loss",
"realizable",
"inherited auditory system disease",
"auditory system disease",
"experimental factor",
"continuant",
"entity",
"autosomal dominant nonsyndromic hearing loss",
"psychiatric disorder",
"auditory system disorder",
"hearing loss disorder",
"hereditary neurological disease",
"hereditary disease",
"nervous system disorder",
"perceptual disorders",
"genetic disorder",
"hearing disorder",
"autosomal dominant disease",
"characteristic",
"hearing loss",
"disposition",
"disease",
"nervous system disease",
"sensory system disease",
"autosomal genetic disease"
],
"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 non-syndromic sensorineural hearing loss type DFNA",
"autosomal dominant isolated sensorineural hearing loss type DFNA",
"autosomal dominant isolated neurosensory hearing loss type DFNA",
"autosomal dominant non-syndromic neurosensory hearing loss type DFNA",
"autosomal dominant nonsyndromic hearing loss",
"autosomal dominant nonsyndromic hearing impairment"
],
"term_id": "MONDO:0019587",
"term_name": "autosomal dominant nonsyndromic hearing loss",
"uuid": "ec02dbab-dbfa-470e-9956-759dc21dc960"
}