{
    "disease_id": "DOID:0070280", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012106", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012106", 
            "name": "microcephaly 5, primary, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012106", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012106", 
            "name": "ASPM autosomal recessive primary microcephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012106", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012106", 
            "name": "autosomal recessive primary microcephaly caused by mutation in ASPM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012106", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012106", 
            "name": "MCPH5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012106", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012106", 
            "name": "microcephaly 5, primary, autosomal recessive; MCPH5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070280", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070280", 
            "name": "MCPH5"
        }, 
        {
            "url": "https://www.omim.org/entry/608716", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608716", 
            "name": "Microcephaly 5, primary, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070280", 
        "description": "A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the ASPM gene on chromosome 1q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070280", 
        "name": "primary autosomal recessive microcephaly 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608716", 
            "id": "608716", 
            "database": "MIM"
        }
    ]
}