{
    "disease_id": "DOID:0111877",
    "recommended_name": {
        "id": "DOID:0111877",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111877",
        "name": "linear skin defects with multiple congenital anomalies 2",
        "description": "A linear skin defects with multiple congenital anomalies characterized by linear skin defects, microcephaly, facial dysmorphism, and other congenital anomalies that has_material_basis_in heterozygous mutation in the COX7B gene on chromosome Xq21.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111877",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111877",
            "name": "APLCC",
            "description": ""
        },
        {
            "id": "DOID:0111877",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111877",
            "name": "LSDMCA2",
            "description": ""
        },
        {
            "id": "DOID:0111877",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111877",
            "name": "aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0010474",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010474",
            "name": "linear skin defects with multiple congenital anomalies 2",
            "description": "Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the COX7B gene."
        },
        {
            "id": "MONDO:0010474",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010474",
            "name": "COX7B microphthalmia with linear skin defects syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010474",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010474",
            "name": "linear skin defects with multiple congenital anomalies 2",
            "description": ""
        },
        {
            "id": "MONDO:0010474",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010474",
            "name": "linear skin defects with multiple congenital anomalies 2, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010474",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010474",
            "name": "linear skin defects with multiple congenital anomalies type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010474",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010474",
            "name": "microphthalmia with linear skin defects syndrome caused by mutation in COX7B",
            "description": ""
        },
        {
            "id": "MONDO:0010474",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010474",
            "name": "LSDMCA2",
            "description": ""
        },
        {
            "id": "MIM:300887",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300887",
            "name": "Linear skin defects with multiple congenital anomalies 2",
            "description": "Linear skin defects with multiple congenital anomalies 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111877"
    ],
    "unlinked_id_list": []
}