{
    "disease_id": "DOID:0110062", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013906", 
            "name": "amelogenesis imperfecta caused by mutation in ODAPH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013906", 
            "name": "amelogenesis imperfecta, hypomaturation type, IIA4; AI2A4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013906", 
            "name": "amelogenesis imperfecta hypomaturation type IIA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013906", 
            "name": "amelogenesis imperfecta type IIA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013906", 
            "name": "ODAPH amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013906", 
            "name": "amelogenesis imperfecta, hypomaturation type, IIA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013906", 
            "name": "AI2A4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110062", 
            "name": "AI2A4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110062", 
            "name": "amelogenesis imperfecta hypomaturation type IIA4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110062", 
            "name": "amelogenesis imperfecta type IIA4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110062", 
        "description": "An amelogenesis imperfecta caused  by homozygous mutation in the C4ORF26 gene on chromosome 4q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110062", 
        "name": "amelogenesis imperfecta hypomaturation type 2A4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110062#disease-associations", 
            "id": "0110062", 
            "database": "Alliance of Genome Resources"
        }
    ]
}