{
    "disease_id": "DOID:0112056", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010496", 
            "name": "MRX12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010496", 
            "name": "mental retardation, X-linked type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010496", 
            "name": "mental retardation, X-linked 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010496", 
            "name": "mental retardation, X-linked 12; MRX12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010496", 
            "name": "mental retardation, X-linked 35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112056", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112056", 
            "name": "MRX12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112056", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112056", 
            "name": "MRX35"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112056", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112056", 
            "name": "X-linked mental retardation 12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112056", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112056", 
            "name": "X-linked mental retardation 35"
        }, 
        {
            "url": "https://www.omim.org/entry/300957", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300957", 
            "name": "Mental retardation, X-linked 12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112056", 
        "description": "A syndromic X-linked intellectual disability characterized by borderline to severe intellectual disability often associated with speech delay, short stature, elevated body mass index, and a truncal obesity pattern in older males that has_material_basis_in hemizygous mutation in THOC2 on chromosome Xq25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112056", 
        "name": "X-linked intellectual disability-short stature-overweight syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300957", 
            "id": "300957", 
            "database": "MIM"
        }
    ]
}