{
    "disease_id": "DOID:0110056",
    "recommended_name": {
        "id": "DOID:0110056",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110056",
        "name": "amelogenesis imperfecta type 1C",
        "description": "An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the enamelin gene (ENAM)."
    },
    "synonyms": [
        {
            "id": "DOID:0110056",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110056",
            "name": "autosomal recessive amelogenesis imperfecta local hypoplastic type",
            "description": ""
        },
        {
            "id": "DOID:0110056",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110056",
            "name": "AI1C",
            "description": ""
        },
        {
            "id": "DOID:0110056",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110056",
            "name": "amelogenesis imperfecta type IC",
            "description": ""
        },
        {
            "id": "DOID:0110056",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110056",
            "name": "autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion",
            "description": ""
        },
        {
            "id": "MONDO:0008770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008770",
            "name": "amelogenesis imperfecta type 1C",
            "description": ""
        },
        {
            "id": "MONDO:0008770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008770",
            "name": "AI1C",
            "description": ""
        },
        {
            "id": "MONDO:0008770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008770",
            "name": "amelogenesis imperfecta type IC",
            "description": ""
        },
        {
            "id": "MONDO:0008770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008770",
            "name": "amelogenesis imperfecta, type 1C",
            "description": ""
        },
        {
            "id": "MONDO:0008770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008770",
            "name": "autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion",
            "description": ""
        },
        {
            "id": "MONDO:0008770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008770",
            "name": "autosomal recessive amelogenesis imperfecta local hypoplastic type",
            "description": ""
        },
        {
            "id": "MONDO:0008770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008770",
            "name": "amelogenesis imperfecta, hypoplastic, with or without Openbite malocclusion, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0008770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008770",
            "name": "amelogenesis imperfecta, local hypoplastic type, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0008770",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008770",
            "name": "amelogenesis imperfecta, type IC",
            "description": ""
        },
        {
            "id": "MIM:204650",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/204650",
            "name": "Amelogenesis imperfecta 1C",
            "description": "Amelogenesis imperfecta 1C"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110056"
    ],
    "unlinked_id_list": []
}