{
    "disease_id": "DOID:0111808", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024552", 
            "name": "microphthalmia, syndromic 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024552", 
            "name": "Midas syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024552", 
            "name": "microphthalmia with linear skin defects"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024552", 
            "name": "HCCS microphthalmia with linear skin defects syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024552", 
            "name": "LSDMCA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024552", 
            "name": "microphthalmia, dermal aplasia, and sclerocornea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024552", 
            "name": "microphthalmia with linear skin defects syndrome caused by mutation in HCCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024552", 
            "name": "linear skin defects with multiple congenital anomalies 1; LSDMCA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111808", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111808", 
            "name": "MCOPS7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111808", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111808", 
            "name": "MIDAS syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111808", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111808", 
            "name": "microphthalmia-dermal aplasia-sclerocornea syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111808", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111808", 
            "name": "MLS syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111808", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111808", 
            "name": "syndromic microphthalmia 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111808", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111808", 
            "name": "syndromic microphthalmia type 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111808", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111808", 
        "name": "linear skin defects with multiple congenital anomalies 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/309801", 
            "id": "309801", 
            "database": "MIM"
        }
    ]
}