{
    "disease_id": "DOID:0111803", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "MMEP syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "MCOPS8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "microphthalmia, syndromic 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "microcephaly, microphthalmia, ectrodactyly of Lower limbs, and prognathism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "microcephaly microphthalmia ectrodactyly of lower limbs and prognathism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "syndromic microphthalmia type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "Viljoen Smart syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "microphthalmia syndromic 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "microphthalmia, syndromic 8; MCOPS8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "Viljoen-Smart syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011045", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011045", 
            "name": "MMEP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111803", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111803", 
            "name": "MCOPS8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111803", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111803", 
            "name": "MMEP syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111803", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111803", 
            "name": "Viljoen-Smart syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111803", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111803", 
            "name": "syndromic microphthalmia type 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111803", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111803", 
            "name": "microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111803", 
        "description": "A syndromic microphthalmia characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs, prognathism and intellectual disability that has_material_basis_in mutation in a region of chromosome 6q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111803", 
        "name": "syndromic microphthalmia 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111803#disease-associations", 
            "id": "0111803", 
            "database": "Alliance of Genome Resources"
        }
    ]
}