{
    "disease_id": "DOID:0081030",
    "recommended_name": {
        "id": "DOID:0081030",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081030",
        "name": "central conducting lymphatic anomaly",
        "description": "A lymphatic system disease that is characterized by dysfunction of the thoracic duct or cisterna chyli, leading to a retrograde flux of lymphatic fluid or abnormal drainage of lymphatic fluid and that has_material_basis_in heterozygous mutation in the EPHB4 gene on chromosome 7q22."
    },
    "synonyms": [
        {
            "id": "DOID:0081030",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081030",
            "name": "lymphatic malformation-7",
            "description": ""
        },
        {
            "id": "MONDO:0015009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015009",
            "name": "lymphatic malformation 7",
            "description": ""
        },
        {
            "id": "MONDO:0015009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015009",
            "name": "HFASD",
            "description": ""
        },
        {
            "id": "MONDO:0015009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015009",
            "name": "hydrops fetalis, nonimmune, and/or atrial septal defect, susceptibility to",
            "description": ""
        },
        {
            "id": "MONDO:0015009",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015009",
            "name": "hydrops fetalis, nonimmune, and/or atrial septal defect, susceptibility to; HFASD",
            "description": ""
        },
        {
            "id": "MONDO:0031043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031043",
            "name": "lymphatic malformation 12",
            "description": ""
        },
        {
            "id": "MONDO:0031043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031043",
            "name": "LMPHM12",
            "description": ""
        },
        {
            "id": "MONDO:0031043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031043",
            "name": "central conducting lymphatic anomaly",
            "description": ""
        },
        {
            "id": "MONDO:0031043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031043",
            "name": "lymphatic malformation 12",
            "description": ""
        },
        {
            "id": "MIM:617300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617300",
            "name": "Lymphatic malformation 7",
            "description": "Lymphatic malformation 7"
        },
        {
            "id": "MIM:620014",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620014",
            "name": "Lymphatic malformation 12",
            "description": "Lymphatic malformation 12"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081030"
    ],
    "unlinked_id_list": []
}