{
    "disease_id": "DOID:0110053",
    "recommended_name": {
        "id": "DOID:0110053",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110053",
        "name": "amelogenesis imperfecta type 4",
        "description": "An amelogenesis imperfecta which can has_material_basis_in mutation in the DLX3 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0110053",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110053",
            "name": "AI4",
            "description": ""
        },
        {
            "id": "DOID:0110053",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110053",
            "name": "AIHHT",
            "description": ""
        },
        {
            "id": "DOID:0110053",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110053",
            "name": "amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism",
            "description": ""
        },
        {
            "id": "MONDO:0007093",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007093",
            "name": "hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism",
            "description": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the DLX3 gene."
        },
        {
            "id": "MONDO:0007093",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007093",
            "name": "AI4",
            "description": ""
        },
        {
            "id": "MONDO:0007093",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007093",
            "name": "AIHHT",
            "description": ""
        },
        {
            "id": "MONDO:0007093",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007093",
            "name": "DLX3 amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0007093",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007093",
            "name": "amelogenesis imperfecta caused by mutation in DLX3",
            "description": ""
        },
        {
            "id": "MONDO:0007093",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007093",
            "name": "amelogenesis imperfecta type 4",
            "description": ""
        },
        {
            "id": "MONDO:0007093",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007093",
            "name": "amelogenesis imperfecta, type IV",
            "description": ""
        },
        {
            "id": "MIM:104510",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/104510",
            "name": "Amelogenesis imperfecta 4",
            "description": "Amelogenesis imperfecta 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110053"
    ],
    "unlinked_id_list": []
}