{
    "disease_id": "DOID:0112106", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010463", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010463", 
            "name": "X-linked dominant chondrodysplasia, Chassaing-Lacombe type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010463", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010463", 
            "name": "X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112106", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112106", 
            "name": "X-linked dominant chondrodysplasia, Chassaing-Lacombe type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112106", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112106", 
            "name": "X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112106", 
        "description": "A syndrome characterized by chondrodysplasia associated with other features including intrauterine growth retardation, hydrocephaly, macrocephaly, frontal bossing, microphthalmia, small low-set ears, and short flat nose that has_material_basis_in heterozygous mutation in HDAC6 on chromosome Xp11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112106", 
        "name": "chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300863", 
            "id": "300863", 
            "database": "MIM"
        }
    ]
}