{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008740", 
            "name": "otocephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008740", 
            "name": "agnathia-holoprosencephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008740", 
            "name": "holoprosencephaly-agnathia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008740", 
            "name": "AGOTC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008740", 
            "name": "agnathia-holoprosencephaly-situs inversus syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008740", 
            "name": "agnathia-otocephaly complex; AGOTC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008740", 
            "name": "dysgnathia complex agnathia-holoprosencephaly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060341", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060341", 
            "name": "agnathia-holoprosencephaly-situs inversus syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060341", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060341", 
            "name": "dysgnathia complex agnathia-holoprosencephaly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060341", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060341", 
            "name": "holoprosencephaly-agnathia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060341", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060341", 
            "name": "otocephaly"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060341", 
        "description": "A physical disorder characterized by mandibular hypoplasia or agnathia, ventromedial auricular malposition (melotia) and/or auricular fusion (synotia), and microstomia with oroglossal hypoplasia or aglossia. Holoprosencephaly is the most commonly identified association, but skeletal, genitourinary and cardiovascular anomalies and situs inversus have been reported.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060341", 
        "name": "agnathia-otocephaly complex"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/202650", 
            "id": "202650", 
            "database": "MIM"
        }
    ]
}