{
    "disease_id": "DOID:0111581", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008893", 
            "name": "OTCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008893", 
            "name": "trigonocephaly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008893", 
            "name": "Opitz trigonocephaly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008893", 
            "name": "Opitz C trigonocephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008893", 
            "name": "trigonocephaly C syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008893", 
            "name": "Opitz trigonocephaly C syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111581", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111581", 
            "name": "OTCS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111581", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111581", 
            "name": "Opitz C trigonocephaly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111581", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111581", 
            "name": "Opitz trigonocephaly C syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111581", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111581", 
            "name": "Opitz trigonocephaly syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111581", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111581", 
            "name": "trigonocephaly C syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111581", 
        "description": "A syndrome characterized by trigonocephaly, psychomotor retardation, hypotonia, variable cardiac defects, redundant skin, and dysmorphic facial features that has_material_basis_in heterozygous mutation in CD96 on chromosome 3q13.1-q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111581", 
        "name": "C syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111581#disease-associations", 
            "id": "0111581", 
            "database": "Alliance of Genome Resources"
        }
    ]
}