{
    "disease_id": "DOID:0111860",
    "recommended_name": {
        "id": "DOID:0111860",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111860",
        "name": "AMME complex",
        "description": "A syndrome characterized by Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis that has_material_basis_in hemizygous deletion of multiple genes including COL4A5, FACL4 and AMMECR1 on chromosome Xq22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111860",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111860",
            "name": "Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111860",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111860",
            "name": "AMME syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111860",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111860",
            "name": "ATS-MR",
            "description": ""
        },
        {
            "id": "DOID:0111860",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111860",
            "name": "chromosome Xq22.3 telomeric deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010263",
            "name": "Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010263",
            "name": "AMME complex",
            "description": ""
        },
        {
            "id": "MONDO:0010263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010263",
            "name": "AMME syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010263",
            "name": "ATS-MR",
            "description": ""
        },
        {
            "id": "MONDO:0010263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010263",
            "name": "Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis",
            "description": ""
        },
        {
            "id": "MIM:300194",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300194",
            "name": "AMME complex",
            "description": "AMME complex"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111860"
    ],
    "unlinked_id_list": []
}