{
    "disease_id": "DOID:2187", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "amelogenesis imperfecta type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "enam amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "amelogenesis imperfecta caused by mutation in ENAM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "amelogenesis imperfecta, type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "amelogenesis imperfecta, type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "AIH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "amelogenesis imperfecta, hypoplastic local, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "hereditary localized enamel hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "enamel hypoplasia, hereditary localized"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "amelogenesis imperfecta type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "autosomal dominant hypoplastic local amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "AI1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007092", 
            "name": "amelogenesis imperfecta, type IB; AI1B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2187", 
        "description": "A dental enamel hypoplasia characterized by abnormal enamel formation.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2187", 
        "name": "amelogenesis imperfecta"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2187#disease-associations", 
            "id": "2187", 
            "database": "Alliance of Genome Resources"
        }
    ]
}