{
    "disease_id": "DOID:0070277", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014660", 
            "name": "microcephaly 15, primary, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014660", 
            "name": "MCPH15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014660", 
            "name": "microcephaly 15, primary, autosomal recessive; MCPH15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070277", 
            "name": "MCPH15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070277", 
            "name": "NEDMISBA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070277", 
            "name": "neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070277", 
        "description": "A primary autosomal recessive microcephaly characterized by impaired intellectual development with poor speech, progressive microcephaly, and appendicular spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the MFSD2A gene on chromosome 1p34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070277", 
        "name": "primary autosomal recessive microcephaly 15"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070277#disease-associations", 
            "id": "0070277", 
            "database": "Alliance of Genome Resources"
        }
    ]
}