{
    "disease_id": "DOID:0060861", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "microphthalmia with limb anomalies; MLA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "anophthalmos-syndactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "anophthalmos with limb anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "OAS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "anophthalmia-syndactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "ophthalmoacromelic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "anophthalmia-syndactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "MLA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "Waardenburg anophthalmia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008800", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008800", 
            "name": "anophthalmia Waardenburg syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060861", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060861", 
            "name": "MLA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060861", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060861", 
            "name": "OAS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060861", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060861", 
            "name": "Waardenburg anophthalmia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060861", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060861", 
            "name": "anophthalmia-syndactyly syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060861", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060861", 
            "name": "ophthalmoacromelic syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060861", 
        "description": "A syndrome that is characterized by autosomal recessive inheritance of bilateral or unilateral clinical anophthalmia or microphthalmia and synostosis, syndactyly, oligodactyly and/or polydactyly that has material_basis_in homozygous mutation in the SMOC1 gene on chromosome 14q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060861", 
        "name": "microphthalmia with limb anomalies"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060861#disease-associations", 
            "id": "0060861", 
            "database": "Alliance of Genome Resources"
        }
    ]
}