{
    "disease_id": "DOID:0111808",
    "recommended_name": {
        "id": "DOID:0111808",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111808",
        "name": "linear skin defects with multiple congenital anomalies 1",
        "description": "A syndromic microphthalmia characterized by unilateral or bilateral microphthalmia and linear skin defects on the face and neck in females and in utero lethality in males that has_material_basis_in heterozygous or hemizygous mutation in HCCS on chromosome Xp22.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111808",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111808",
            "name": "MCOPS7",
            "description": ""
        },
        {
            "id": "DOID:0111808",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111808",
            "name": "MIDAS syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111808",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111808",
            "name": "microphthalmia-dermal aplasia-sclerocornea syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111808",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111808",
            "name": "MLS syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111808",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111808",
            "name": "syndromic microphthalmia 7",
            "description": ""
        },
        {
            "id": "DOID:0111808",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111808",
            "name": "syndromic microphthalmia type 7",
            "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": "microphthalmia, syndromic 7",
            "description": ""
        },
        {
            "id": "MONDO:0024552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024552",
            "name": "Midas syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024552",
            "name": "microphthalmia with linear skin defects",
            "description": ""
        },
        {
            "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": "LSDMCA1",
            "description": ""
        },
        {
            "id": "MONDO:0024552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024552",
            "name": "microphthalmia, dermal aplasia, and sclerocornea",
            "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": "linear skin defects with multiple congenital anomalies 1; 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"
        }
    ]
}