{
    "disease_id": "DOID:0110066", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta caused by mutation in FAM20A"
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        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta nephrocalcinosis"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "ers"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta, type 1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta-nephrocalcinosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "FAM20A amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "generalized enamel hypoplasia and renal dysfunction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta, hypoplastic, with nephrocalcinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "AI1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta type Ig"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta, type Ig; AI1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "enamel-renal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta and gingival fibromatosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta and nephrocalcinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta hypoplastic type, Ig"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "enamel renal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "AIGFS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "amelogenesis imperfecta hypoplastic with nephrocalcinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "enamel-renal-gingival syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008771", 
            "name": "absent enamel, nephrocalcinosis and apparently normal calcium metabolism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110066", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110066", 
            "name": "amelogenesis imperfecta and gingival fibromatosis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110066", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110066", 
            "name": "amelogenesis imperfecta hypoplastic with nephrocalcinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110066", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110066", 
            "name": "AI1G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110066", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110066", 
            "name": "AIGFS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110066", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110066", 
            "name": "ERS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110066", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110066", 
            "name": "amelogenesis imperfecta type IG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110066", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110066", 
            "name": "enamel-renal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110066", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110066", 
            "name": "enamel-renal-gingival syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110066", 
        "description": "An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110066", 
        "name": "amelogenesis imperfecta type 1G"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110066#disease-associations", 
            "id": "0110066", 
            "database": "Alliance of Genome Resources"
        }
    ]
}