{
    "disease_id": "DOID:0110489",
    "recommended_name": {
        "id": "DOID:0110489",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110489",
        "name": "autosomal recessive nonsyndromic deafness 30",
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutations in the MYO3A gene on chromosome 10p12.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110489",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110489",
            "name": "DFNB30",
            "description": ""
        },
        {
            "id": "DOID:0110489",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110489",
            "name": "autosomal recessive deafness 30",
            "description": ""
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "autosomal recessive nonsyndromic hearing loss 30",
            "description": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO3A gene."
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "autosomal recessive nonsyndromic hearing loss 30",
            "description": ""
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "DFNB30",
            "description": ""
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "MYO3A autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "autosomal recessive deafness 30",
            "description": ""
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "autosomal recessive nonsyndromic deafness 30",
            "description": ""
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in MYO3A",
            "description": ""
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "autosomal recessive nonsyndromic deafness type 30",
            "description": ""
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "deafness, autosomal recessive 30",
            "description": ""
        },
        {
            "id": "MONDO:0011774",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011774",
            "name": "deafness, autosomal recessive type 30",
            "description": ""
        },
        {
            "id": "MIM:607101",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607101",
            "name": "Deafness, autosomal recessive, 30",
            "description": "Deafness, autosomal recessive, 30"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110489"
    ],
    "unlinked_id_list": []
}