{
    "disease_id": "DOID:0111580", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008858", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008858", 
            "name": "optic atrophy, infantile hereditary, with neurologic abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008858", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008858", 
            "name": "optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008858", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008858", 
            "name": "Behr syndrome; BEHRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008858", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008858", 
            "name": "BEHRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008858", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008858", 
            "name": "optic atrophy, infantile hereditary, Behr complicated form of"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111580", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111580", 
            "name": "Abortive cerebellar ataxia (BEHRS)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111580", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111580", 
            "name": "BEHRS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111580", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111580", 
            "name": "optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111580", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111580", 
            "name": "optic atrophy, infantile hereditary, Behr complicated form of"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111580", 
        "description": "A nervous system disease characterized by early-onset optic atrophy, ataxia, pyramidal signs, spasticity, and intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in OPA1 on chromosome 3q29.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111580", 
        "name": "Behr syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/210000", 
            "id": "210000", 
            "database": "MIM"
        }
    ]
}