{
    "disease_id": "DOID:0111860", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010263", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010263", 
            "name": "Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010263", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010263", 
            "name": "ATS-MR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010263", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010263", 
            "name": "chromosome Xq22.3 telomeric deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010263", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010263", 
            "name": "AMME syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010263", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010263", 
            "name": "Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111860", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111860", 
            "name": "ATS-MR"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111860", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111860", 
            "name": "Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111860", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111860", 
            "name": "AMME syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111860", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111860", 
            "name": "chromosome Xq22.3 telomeric deletion syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111860", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111860", 
        "name": "AMME complex"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111860#disease-associations", 
            "id": "0111860", 
            "database": "Alliance of Genome Resources"
        }
    ]
}