{
    "disease_id": "DOID:0110054",
    "recommended_name": {
        "id": "DOID:0110054",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110054",
        "name": "amelogenesis imperfecta type 1A",
        "description": "An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32."
    },
    "synonyms": [
        {
            "id": "DOID:0110054",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110054",
            "name": "AI1A",
            "description": ""
        },
        {
            "id": "DOID:0110054",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110054",
            "name": "amelogenesis imperfecta hypoplastic type IA",
            "description": ""
        },
        {
            "id": "DOID:0110054",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110054",
            "name": "amelogenesis imperfecta type IA",
            "description": ""
        },
        {
            "id": "MONDO:0007094",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007094",
            "name": "amelogenesis imperfecta type 1A",
            "description": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the LAMB3 gene."
        },
        {
            "id": "MONDO:0007094",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007094",
            "name": "AI1A",
            "description": ""
        },
        {
            "id": "MONDO:0007094",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007094",
            "name": "LAMB3 amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0007094",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007094",
            "name": "amelogenesis imperfecta caused by mutation in LAMB3",
            "description": ""
        },
        {
            "id": "MONDO:0007094",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007094",
            "name": "amelogenesis imperfecta local hypoplastic",
            "description": ""
        },
        {
            "id": "MONDO:0007094",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007094",
            "name": "amelogenesis imperfecta, type IA",
            "description": ""
        },
        {
            "id": "MONDO:0007094",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007094",
            "name": "local hypoplastic amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MIM:104530",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/104530",
            "name": "Amelogenesis imperfecta 1A",
            "description": "Amelogenesis imperfecta 1A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110054"
    ],
    "unlinked_id_list": []
}