{
    "disease_id": "DOID:0111875",
    "recommended_name": {
        "id": "DOID:0111875",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111875",
        "name": "MLS syndrome",
        "description": "A syndrome characterized by linear skin defects and various other congenital anomalies. The classical diagnosis consisted of unilateral or bilateral microphthalmia and/or anophthalmia and linear skin defects but patients with a molecular diagnosis of MLS syndrome may not display eye abnormalities."
    },
    "synonyms": [
        {
            "id": "DOID:0111875",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111875",
            "name": "linear skin defects with multiple congenital anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0024552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024552",
            "name": "linear skin defects with multiple congenital anomalies 1",
            "description": "Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the HCCS gene."
        },
        {
            "id": "MONDO:0024552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024552",
            "name": "HCCS microphthalmia with linear skin defects syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024552",
            "name": "linear skin defects with multiple congenital anomalies 1",
            "description": ""
        },
        {
            "id": "MONDO:0024552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024552",
            "name": "linear skin defects with multiple congenital anomalies 1, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0024552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024552",
            "name": "microphthalmia with linear skin defects syndrome caused by mutation in HCCS",
            "description": ""
        },
        {
            "id": "MONDO:0024552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024552",
            "name": "LSDMCA1",
            "description": ""
        },
        {
            "id": "MIM:309801",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/309801",
            "name": "Linear skin defects with multiple congenital anomalies 1",
            "description": "Linear skin defects with multiple congenital anomalies 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0111808",
            "label": "linear skin defects with multiple congenital anomalies 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111876",
            "label": "linear skin defects with multiple congenital anomalies 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111877",
            "label": "linear skin defects with multiple congenital anomalies 2",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0111876",
        "DOID:0111877",
        "DOID:0111808",
        "DOID:0111875"
    ],
    "unlinked_id_list": []
}