{
    "disease_id": "DOID:0060341",
    "recommended_name": {
        "id": "DOID:0060341",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060341",
        "name": "agnathia-otocephaly complex",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060341",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060341",
            "name": "agnathia-holoprosencephaly-situs inversus syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060341",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060341",
            "name": "dysgnathia complex agnathia-holoprosencephaly",
            "description": ""
        },
        {
            "id": "DOID:0060341",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060341",
            "name": "holoprosencephaly-agnathia",
            "description": ""
        },
        {
            "id": "DOID:0060341",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060341",
            "name": "otocephaly",
            "description": ""
        },
        {
            "id": "MONDO:0008740",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008740",
            "name": "agnathia-otocephaly complex",
            "description": "Agnathia-holoprosencephaly-situs inversus syndrome is an extremely rare and fatal association syndrome, characterized by absence of the mandible, cerebral malformations with facial anomalies related to a defect in cleavage in the embryonic brain (e.g. synophthalmia, malformed and low-set ears fused in midline (otocephaly), agenesis of the olfactory bulbs, microstomia, hypoglossia/aglossia) and situs inversus partialis or totalis."
        },
        {
            "id": "MONDO:0008740",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008740",
            "name": "agnathia-holoprosencephaly-situs inversus syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008740",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008740",
            "name": "agnathia-otocephaly complex",
            "description": ""
        },
        {
            "id": "MONDO:0008740",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008740",
            "name": "dysgnathia complex agnathia-holoprosencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0008740",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008740",
            "name": "holoprosencephaly-agnathia",
            "description": ""
        },
        {
            "id": "MONDO:0008740",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008740",
            "name": "otocephaly",
            "description": ""
        },
        {
            "id": "MONDO:0008740",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008740",
            "name": "AGOTC",
            "description": ""
        },
        {
            "id": "MONDO:0008740",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008740",
            "name": "agnathia-holoprosencephaly",
            "description": ""
        },
        {
            "id": "MIM:202650",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/202650",
            "name": "Agnathia-otocephaly complex",
            "description": "Agnathia-otocephaly complex"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060341"
    ],
    "unlinked_id_list": []
}