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