{
    "disease_id": "DOID:0110055", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta, type 3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "autosomal dominant amelogenesis imperfecta hypocalcification type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta caused by mutation in FAM83H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "AI3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "FAM83H amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta, type IIIA; AI3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta, hypocalcification type, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta hypomineralization type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "AI3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta, type III; AI3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "ADHCAI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007538", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007538", 
            "name": "amelogenesis imperfecta, hypomineralization type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110055", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110055", 
            "name": "ADHCAI"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110055", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110055", 
            "name": "AI3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110055", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110055", 
            "name": "amelogenesis imperfecta hypomineralization type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110055", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110055", 
            "name": "amelogenesis imperfecta type III"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110055", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110055", 
            "name": "autosomal dominant amelogenesis imperfecta hypocalcification type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110055", 
        "description": "An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110055", 
        "name": "amelogenesis imperfecta type 3A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110055#disease-associations", 
            "id": "0110055", 
            "database": "Alliance of Genome Resources"
        }
    ]
}