{
    "disease_id": "DOID:0051037",
    "recommended_name": {
        "id": "DOID:0051037",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051037",
        "name": "autosomal dominant primary microcephaly 26",
        "description": "A primary microcephaly that is characterized by progressive microcephaly beginning at birth and associated with global developmental delay with variably impaired intellectual development and that has_material_basis_in heterozygous mutation in the LMNB1 gene on chromosome 5q23."
    },
    "synonyms": [
        {
            "id": "MONDO:0030928",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030928",
            "name": "microcephaly 26, primary, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0030928",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030928",
            "name": "MCPH26",
            "description": ""
        },
        {
            "id": "MONDO:0030928",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030928",
            "name": "microcephaly 26, primary, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:619179",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619179",
            "name": "Microcephaly 26, primary, autosomal dominant",
            "description": "Microcephaly 26, primary, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051037"
    ],
    "unlinked_id_list": []
}