{
    "disease_id": "DOID:0060815", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010758", 
            "name": "intellectual disability-developmental delay-contractures syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010758", 
            "name": "WRWF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010758", 
            "name": "foot contractures-muscle atrophy-oculomotor apraxia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010758", 
            "name": "WIEACKER-WOLFF syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010758", 
            "name": "apraxia, oculomotor, with congenital contractures and muscle atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010758", 
            "name": "Wieacker Wolff syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010758", 
            "name": "Wieacker syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010758", 
            "name": "contractures of feet, muscle atrophy, and oculomotor apraxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010758", 
            "name": "WIEACKER-WOLFF syndrome; WRWF"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060815", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060815", 
            "name": "MCS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060815", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060815", 
            "name": "MRXS4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060815", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060815", 
            "name": "mental retardation, X-linked, syndromic 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060815", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060815", 
            "name": "X-linked intellectual disability, Miles-Carpenter type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060815", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060815", 
            "name": "mental retardation, X-linked, with congenital contractures and low fingertip arches"
        }, 
        {
            "url": "https://www.omim.org/entry/314580", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:314580", 
            "name": "Wieacker-Wolf syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060815", 
        "description": "A syndromic X-linked intellectual disability characterized by severe intellectual deficit, microcephaly, exotropia, distal muscle wasting and low digital arches that has_material_basis_in variation in chromosomal region Xq13-q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060815", 
        "name": "Miles-Carpenter syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/314580", 
            "id": "314580", 
            "database": "MIM"
        }
    ]
}