{
    "disease_id": "DOID:0060609", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "microcephalic osteodysplastic primordial dwarfism type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "microcephalic osteodysplastic primordial dwarfism, type II; MOPD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "osteodysplastic primordial dwarfism type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "Mopd 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "microcephalic osteodysplastic primordial dwarfism, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "MOPD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "microcephalic osteodysplastic primordial dwarfism with tooth abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "microcephalic osteodysplastic primordial dwarfism, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "MOPD II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "osteodysplastic primordial dwarfism, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "osteodysplastic primordial dwarfism type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "Majewski osteodysplastic primordial dwarfism type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008872", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008872", 
            "name": "MOPD type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060609", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060609", 
            "name": "osteodysplastic primordial dwarfism type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060609", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060609", 
            "name": "Majewski osteodysplastic primordial dwarfism type II"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060609", 
        "description": "A microcephalic osteodysplastic primordial dwarfism that has_material_basis_in homozygous or compound heterozygous mutation in the PCNT gene, encoding pericentrin, on chromosome 21q22. It is characterized by intrauterine growth retardation, severe proportionate short stature, and microcephaly.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060609", 
        "name": "microcephalic osteodysplastic primordial dwarfism type II"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060609#disease-associations", 
            "id": "0060609", 
            "database": "Alliance of Genome Resources"
        }
    ]
}