{
    "disease_id": "DOID:0111805", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "microphthalmia with brain and digit anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "microphthalmia syndromic 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "Bakrania-Ragge syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "anophthalmia, clinical, with micrognathia, malformed ears, digital anomalies, and abnormal external genitalia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "microphthalmia, syndromic type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "microphthalmia and pituitary anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "microphthalmia, syndromic 6; MCOPS6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "syndromic microphthalmia type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "microphthalmia, syndromic 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "MCOPS6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "microphthalmia with brain and digit developmental anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011936", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011936", 
            "name": "anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111805", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111805", 
            "name": "MCOPS6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111805", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111805", 
            "name": "Bakrania-Ragge syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111805", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111805", 
            "name": "microphthalmia and pituitary anomalies"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111805", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111805", 
            "name": "microphthalmia with brain and digit anomalies"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111805", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111805", 
            "name": "anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111805", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111805", 
            "name": "syndromic microphthalmia type 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111805", 
        "description": "A syndromic microphthalmia characterized by clinical anophthalmia or microphthalmia, retinal dystrophy, and/or myopia, associated in some cases with cerebral anomalies that has_material_basis_in heterozygous mutation in BMP4 on chromosome 14q22.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111805", 
        "name": "syndromic microphthalmia 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111805#disease-associations", 
            "id": "0111805", 
            "database": "Alliance of Genome Resources"
        }
    ]
}