{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "pseudo-TORCH syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "bilateral band-like calcification with polymicrogyria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "microcephaly-intracranial calcification-intellectual disability syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "band-like calcification with simplified gyration and polymicrogyria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "BLCPMG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "pseudo-TORCH syndrome 1; PTORCH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "Baraitser-Brett-Piesowicz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "congenital intrauterine infection-like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "microcephaly - intracranial calcification - intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "Baraitser Brett Piesowicz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "microcephaly intracranial calcification"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "pseudo-TORCH syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "Baraitser-Reardon syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "PTORCH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "band-like calcification with simplified gyration and polymicrogyria; BLCPMG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009626", 
            "name": "BLC-PMG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050656", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050656", 
            "name": "microcephaly-intracranial calcification-intellectual disability syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050656", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050656", 
            "name": "bilateral band-like calcification with polymicrogyria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050656", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050656", 
            "name": "BLC-PMG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050656", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050656", 
            "name": "BLCPMG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050656", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050656", 
            "name": "Baraitser-Brett-Piesowicz syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050656", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050656", 
            "name": "Baraitser-Reardon syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050656", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050656", 
            "name": "PTORCH1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050656", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050656", 
            "name": "band-like calcification with simplified gyration and polymicrogyria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050656", 
        "description": "A syndrome that is characterized by congenital microcephaly, intracranial calcifications, severe developmental delay, simplified gyration and polymicrogyria that has_material_basis_in homozygous or compound heterozygous mutation in OCLN on chromosome 5q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050656", 
        "name": "pseudo-TORCH syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/251290", 
            "id": "251290", 
            "database": "MIM"
        }
    ]
}