{
    "disease_id": "DOID:0110060",
    "recommended_name": {
        "id": "DOID:0110060",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110060",
        "name": "amelogenesis imperfecta hypomaturation type 2A2",
        "description": "An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the matrix metalloproteinase-20 gene (MMP20)."
    },
    "synonyms": [
        {
            "id": "DOID:0110060",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110060",
            "name": "AI2A2",
            "description": ""
        },
        {
            "id": "DOID:0110060",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110060",
            "name": "amelogenesis imperfecta hypomaturation type IIA2",
            "description": ""
        },
        {
            "id": "DOID:0110060",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110060",
            "name": "amelogenesis imperfecta type IIA2",
            "description": ""
        },
        {
            "id": "DOID:0110060",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110060",
            "name": "amelogenesis imperfecta pigmented hypomaturation type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012926",
            "name": "amelogenesis imperfecta hypomaturation type 2A2",
            "description": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the MMP20 gene."
        },
        {
            "id": "MONDO:0012926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012926",
            "name": "AI2A2",
            "description": ""
        },
        {
            "id": "MONDO:0012926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012926",
            "name": "MMP20 amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0012926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012926",
            "name": "amelogenesis imperfecta caused by mutation in MMP20",
            "description": ""
        },
        {
            "id": "MONDO:0012926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012926",
            "name": "amelogenesis imperfecta, type IIA2",
            "description": ""
        },
        {
            "id": "MONDO:0012926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012926",
            "name": "amelogenesis imperfecta, hypomaturation type, IIA2",
            "description": ""
        },
        {
            "id": "MIM:612529",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612529",
            "name": "Amelogenesis imperfecta, hypomaturation type, 2A2",
            "description": "Amelogenesis imperfecta, hypomaturation type, 2A2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110060"
    ],
    "unlinked_id_list": []
}