{
    "disease_id": "DOID:0110061",
    "recommended_name": {
        "id": "DOID:0110061",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110061",
        "name": "amelogenesis imperfecta hypomaturation type 2A3",
        "description": "An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0110061",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110061",
            "name": "AI2A3",
            "description": ""
        },
        {
            "id": "DOID:0110061",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110061",
            "name": "amelogenesis imperfecta hypomaturation type IIA3",
            "description": ""
        },
        {
            "id": "DOID:0110061",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110061",
            "name": "amelogenesis imperfecta type IIA3",
            "description": ""
        },
        {
            "id": "MONDO:0013181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013181",
            "name": "amelogenesis imperfecta hypomaturation type 2A3",
            "description": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the WDR72 gene."
        },
        {
            "id": "MONDO:0013181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013181",
            "name": "AI2A3",
            "description": ""
        },
        {
            "id": "MONDO:0013181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013181",
            "name": "WDR72 amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0013181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013181",
            "name": "amelogenesis imperfecta caused by mutation in WDR72",
            "description": ""
        },
        {
            "id": "MONDO:0013181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013181",
            "name": "amelogenesis imperfecta hypomaturation type 2A3",
            "description": ""
        },
        {
            "id": "MONDO:0013181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013181",
            "name": "amelogenesis imperfecta, type IIA3",
            "description": ""
        },
        {
            "id": "MONDO:0013181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013181",
            "name": "amelogenesis imperfecta, hypomaturation type, IIA3",
            "description": ""
        },
        {
            "id": "MIM:613211",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613211",
            "name": "Amelogenesis imperfecta, hypomaturation type, 2A3",
            "description": "Amelogenesis imperfecta, hypomaturation type, 2A3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110061"
    ],
    "unlinked_id_list": []
}