{
    "disease_id": "DOID:0090132", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "PMGYSA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "polymicrogyria, symmetric or asymmetric; PMGYSA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "cortical dysplasia, Complex, with Other brain malformations 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "cortical dysplasia, COMPLEX, with OTHER brain malformations 7; CDCBM7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "polymicrogyria, symmetric or asymmetric"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "TUBB2B complex cortical dysplasia with other brain malformations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "polymicrogyria due to TUBB2B mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "complex cortical dysplasia with other brain malformations caused by mutation in TUBB2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "complex cortical dysplasia with other brain malformations type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012399", 
            "name": "CDCBM7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090132", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090132", 
            "name": "CDCBM7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090132", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090132", 
            "name": "polymicrogyria due to TUBB2B mutation"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090132", 
        "description": "A complex cortical dysplasia with other brain malformations that is characterized by abnromalities in coritcal brain development that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin beta 2B class IIb (TUBB2B) gene on chromosome 6p25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090132", 
        "name": "complex cortical dysplasia with other brain malformations 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090132#disease-associations", 
            "id": "0090132", 
            "database": "Alliance of Genome Resources"
        }
    ]
}