{
    "disease_id": "DOID:0111807", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011010", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "Matthew-wood syndrome"
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011010", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011010", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011010", 
            "name": "spear syndrome"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011010", 
            "name": "microphthalmia, isolated, with coloboma 8"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011010", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "anophthalmia-pulmonary hypoplasia syndrome"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "microphthalmia, syndromic 9"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "anophthalmia/microphthalmia and pulmonary hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011010", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011010", 
            "name": "pulmonary Hypoplasia-diaphragmatic hernia-anophthalmia-Cardiac defect"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "microphthalmia syndromic type 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111807", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111807", 
            "name": "Matthew-Wood syndrome"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111807", 
            "name": "pulmonary agenesis microphthalmi and diaphragmatic defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111807", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111807", 
            "name": "anophthalmia-pulmonary hypoplasia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111807", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111807", 
            "name": "spear syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111807", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111807", 
            "name": "anophthalmia/microphthalmia and pulmonary hypoplasia"
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        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111807", 
            "name": "clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
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            "name": "Microphthalmia, syndromic, 9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111807", 
        "description": "A syndromic microphthalmia characterized by bilateral clinical anophthalmia, pulmonary hypoplasia or aplasia, cardiac malformations, and diaphragmatic defects that has_material_basis_in homozygous or compound heterozygous mutation in STRA6 on chromosome 15q24.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111807", 
        "name": "syndromic microphthalmia 9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/601186", 
            "id": "601186", 
            "database": "MIM"
        }
    ]
}