{
    "disease_id": "DOID:2340", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:2340", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2340", 
            "name": "Premature closure of cranial sutures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014128", 
            "description": "Any craniosynostosis in which the cause of the disease is a mutation in the TCF12 gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0014128", 
            "name": "craniosynostosis 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014128", 
            "name": "craniosynostosis type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014128", 
            "name": "craniosynostosis caused by mutation in TCF12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014128", 
            "name": "TCF12 craniosynostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014128", 
            "name": "CRS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014128", 
            "name": "craniosynostosis 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014128", 
            "name": "craniosynostosis 3; CRS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "Craniosynostosis, Boston type is a form of syndromic craniosynostosis (see this term), 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.", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "craniosynostosis, Boston type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "Warman Mulliken Hayward syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "CRS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "craniosynostosis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "Warman-Mulliken-Hayward syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "craniosynostosis Boston type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "craniosynostosis 2; CRS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "craniosynostosis 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "craniosynostosis, Warman type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "craniosynostosis Warman type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011481", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011481", 
            "name": "craniosynostosis, Boston-type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010929", 
            "description": "Any craniosynostosis in which the cause of the disease is a mutation in the ERF gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0010929", 
            "name": "craniosynostosis 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010929", 
            "name": "craniosynostosis caused by mutation in ERF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010929", 
            "name": "ERF craniosynostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010929", 
            "name": "craniosynostosis 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010929", 
            "name": "craniosynostosis 4; CRS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010929", 
            "name": "CRS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010929", 
            "name": "craniosynostosis type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010903", 
            "name": "craniosynostosis, Adelaide type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010903", 
            "name": "craniosynostosis, Adelaide type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010903", 
            "name": "CRSA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010903", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010903", 
            "name": "craniosynostosis, Adelaide type; CRSA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "Shprintzen-Goldberg syndrome (SGS) is a very rare genetic disorder characterized by craniosynostosis, craniofacial and skeletal abnormalities, marfanoid habitus, cardiac anomalies, neurological abnormalities, and intellectual disability.", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "Shprintzen-Goldberg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "Shprintzen-Goldberg marfanoid syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "Marfanoid craniosynostosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "Marfanoid disorder with craniosynostosis, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "Shprintzen-Goldberg craniosynostosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "SGS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "craniosynostosis with arachnodactyly and abdominal hernias"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "Marfanoid disorder with craniosynostosis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "Marfanoid-craniosynostosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008426", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008426", 
            "name": "Shprintzen-Goldberg craniosynostosis syndrome; SGS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007399", 
            "name": "craniosynostosis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007399", 
            "name": "CRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007399", 
            "name": "craniosynostosis 1; CRS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007399", 
            "name": "craniosynostosis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007399", 
            "name": "CRS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007399", 
            "name": "craniosynostosis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007399", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007399", 
            "name": "craniostenosis"
        }, 
        {
            "url": "https://www.omim.org/entry/615314", 
            "description": "Craniosynostosis 3", 
            "resource": "MIM", 
            "id": "MIM:615314", 
            "name": "Craniosynostosis 3"
        }, 
        {
            "url": "https://www.omim.org/entry/604757", 
            "description": "Craniosynostosis 2", 
            "resource": "MIM", 
            "id": "MIM:604757", 
            "name": "Craniosynostosis 2"
        }, 
        {
            "url": "https://www.omim.org/entry/600775", 
            "description": "Craniosynostosis 4", 
            "resource": "MIM", 
            "id": "MIM:600775", 
            "name": "Craniosynostosis 4"
        }, 
        {
            "url": "https://www.omim.org/entry/182212", 
            "description": "Shprintzen-Goldberg craniosynostosis syndrome", 
            "resource": "MIM", 
            "id": "MIM:182212", 
            "name": "Shprintzen-Goldberg craniosynostosis syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/123100", 
            "description": "Craniosynostosis 1", 
            "resource": "MIM", 
            "id": "MIM:123100", 
            "name": "Craniosynostosis 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2340", 
        "description": "A synostosis that results_in premature fusion located_in skull.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2340", 
        "name": "craniosynostosis"
    }
}