{
    "disease_id": "DOID:0061009",
    "recommended_name": {
        "id": "DOID:0061009",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061009",
        "name": "craniosynostosis 2",
        "description": "A craniosynostosis characterized by a highly variable craniosynostosis with frontal bossing, turribrachycephaly and cloverleaf skull anomaly that has_material_basis_in heterozygous mutation in the MSX2 gene on chromosome 5q35."
    },
    "synonyms": [
        {
            "id": "DOID:0061009",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061009",
            "name": "CRS2",
            "description": ""
        },
        {
            "id": "DOID:0061009",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061009",
            "name": "Craniosynostosis Boston type",
            "description": ""
        },
        {
            "id": "DOID:0061009",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061009",
            "name": "Craniosynostosis Warman type",
            "description": ""
        },
        {
            "id": "DOID:0061009",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061009",
            "name": "Warman-Mulliken-Hayward syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011481",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011481",
            "name": "craniosynostosis 2",
            "description": "A form of syndromic craniosynostosis, characterized by a highly variable craniosynostosis with frontal bossing, turribrachycephaly and cloverleaf skull anomaly. Hypoplasia of the supraorbital ridges, cleft palate, extra teeth and limb anomalies (triphalangeal thumb, 3-4 syndactyly of the hands, a short first metatarsal, middle phalangeal agenesis in the feet) have also been described. Associated problems include headache, poor vision, and seizures. Intelligence is normal."
        },
        {
            "id": "MONDO:0011481",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011481",
            "name": "CRS2",
            "description": ""
        },
        {
            "id": "MONDO:0011481",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011481",
            "name": "MSX2-related craniosynostosis",
            "description": ""
        },
        {
            "id": "MONDO:0011481",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011481",
            "name": "Warman-Mulliken-Hayward syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011481",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011481",
            "name": "craniosynostosis 2",
            "description": ""
        },
        {
            "id": "MONDO:0011481",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011481",
            "name": "craniosynostosis type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011481",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011481",
            "name": "craniosynostosis, Warman type",
            "description": ""
        },
        {
            "id": "MONDO:0011481",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011481",
            "name": "Warman Mulliken Hayward syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011481",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011481",
            "name": "craniosynostosis Warman type",
            "description": ""
        },
        {
            "id": "MIM:604757",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604757",
            "name": "Craniosynostosis 2",
            "description": "Craniosynostosis 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061009"
    ],
    "unlinked_id_list": []
}