{
    "disease_id": "DOID:0110054", 
    "synonyms": [
        {
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            "description": "", 
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            "name": "AI1A"
        }, 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007094", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007094", 
            "name": "LAMB3 amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007094", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007094", 
            "name": "amelogenesis imperfecta, type IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007094", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007094", 
            "name": "amelogenesis imperfecta, hypoplastic type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007094", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007094", 
            "name": "amelogenesis imperfecta caused by mutation in LAMB3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007094", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007094", 
            "name": "amelogenesis imperfecta local hypoplastic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007094", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007094", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007094", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007094", 
            "name": "amelogenesis imperfecta, type IA; AI1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110054", 
            "name": "AI1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110054", 
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        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110054", 
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        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:104530", 
            "name": "Amelogenesis imperfecta 1A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110054", 
        "description": "An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32.", 
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        "id": "DOID:0110054", 
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    }, 
    "evidence": [
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            "database": "MIM"
        }
    ]
}