{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "facio-oculo-acoustico-renal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "diaphragmatic hernia-exomphalos-hypertelorism syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "Holmes-Schepens syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and proteinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "syndrome of ocular and facial anomalies, telecanthus and deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "faciooculoacousticorenal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "DBS/FOAR syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "diaphragmatic hernia exomphalos absent corpus callosum hypertelorism myopia sensorineural deafness and proteinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "diaphragmatic hernia-hypertelorism-myopia-deafness syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009104", 
            "name": "FOAR syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090144", 
            "name": "syndrome of ocular and facial anomalies, telecanthus and deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090144", 
            "name": "DBS/FOAR syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090144", 
            "name": "FOAR syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090144", 
            "name": "Holmes-Schepens syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090144", 
            "name": "facio-oculo-acoustico-renal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090144", 
            "name": "faciooculoacousticorenal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090144", 
            "name": "diaphragmatic hernia-hypertelorism-myopia-deafness syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090144", 
            "name": "diaphragmatic hernia-exomphalos-hypertelorism syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090144", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090144", 
            "name": "diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and proteinuria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090144", 
        "description": "A syndrome that is characterized by facial and ocular abnormalities, sensorineural hearing loss, agenesis of the corpus callosum, variable intellectual disability, and proteinuria that has_material_basis_in homozygous or compound heterozygous mutation in the LDL receptor related protein 2 gene (LRP2) on chromosome 2q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090144", 
        "name": "Donnai-Barrow syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/222448", 
            "id": "222448", 
            "database": "MIM"
        }
    ]
}