{
    "disease_id": "DOID:0110062",
    "recommended_name": {
        "id": "DOID:0110062",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110062",
        "name": "amelogenesis imperfecta hypomaturation type 2A4",
        "description": "An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110062",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110062",
            "name": "AI2A4",
            "description": ""
        },
        {
            "id": "DOID:0110062",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110062",
            "name": "amelogenesis imperfecta hypomaturation type IIA4",
            "description": ""
        },
        {
            "id": "DOID:0110062",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110062",
            "name": "amelogenesis imperfecta type IIA4",
            "description": ""
        },
        {
            "id": "MONDO:0013906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013906",
            "name": "amelogenesis imperfecta hypomaturation type 2A4",
            "description": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the ODAPH gene."
        },
        {
            "id": "MONDO:0013906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013906",
            "name": "AI2A4",
            "description": ""
        },
        {
            "id": "MONDO:0013906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013906",
            "name": "ODAPH amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0013906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013906",
            "name": "amelogenesis imperfecta caused by mutation in ODAPH",
            "description": ""
        },
        {
            "id": "MONDO:0013906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013906",
            "name": "amelogenesis imperfecta hypomaturation type IIA4",
            "description": ""
        },
        {
            "id": "MONDO:0013906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013906",
            "name": "amelogenesis imperfecta type IIA4",
            "description": ""
        },
        {
            "id": "MONDO:0013906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013906",
            "name": "amelogenesis imperfecta, type IIA4",
            "description": ""
        },
        {
            "id": "MONDO:0013906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013906",
            "name": "amelogenesis imperfecta, hypomaturation type, IIA4",
            "description": ""
        },
        {
            "id": "MIM:614832",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614832",
            "name": "Amelogenesis imperfecta, hypomaturation type, 2A4",
            "description": "Amelogenesis imperfecta, hypomaturation type, 2A4"
        }
    ]
}