{
    "disease_id": "DOID:0110063", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014385", 
            "name": "amelogenesis imperfecta type IIA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014385", 
            "name": "amelogenesis imperfecta hypomaturation type IIA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014385", 
            "name": "amelogenesis imperfecta, hypomaturation type, IIA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014385", 
            "name": "AI2A5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014385", 
            "name": "SLC24A4 amelogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014385", 
            "name": "amelogenesis imperfecta, hypomaturation type, IIA5; AI2A5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014385", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014385", 
            "name": "amelogenesis imperfecta caused by mutation in SLC24A4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110063", 
            "name": "AI2A5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110063", 
            "name": "amelogenesis imperfecta hypomaturation type IIA5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110063", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110063", 
            "name": "amelogenesis imperfecta type IIA5"
        }, 
        {
            "url": "https://www.omim.org/entry/615887", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615887", 
            "name": "Amelogenesis imperfecta, hypomaturation type, 2A5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110063", 
        "description": "An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the SLC24A4 gene on chromosome 14q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110063", 
        "name": "amelogenesis imperfecta hypomaturation type 2A5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615887", 
            "id": "615887", 
            "database": "MIM"
        }
    ]
}