{
    "disease_id": "DOID:0060703", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011274", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011274", 
            "name": "FGFR3-related craniosynostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011274", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011274", 
            "name": "syndrome of coronal craniosynostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011274", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011274", 
            "name": "MNKES"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011274", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011274", 
            "name": "Muenke nonsyndromic coronal craniosynostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011274", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011274", 
            "name": "Muenke syndrome; MNKES"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060703", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060703", 
            "name": "FGFR3-related craniosynostosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060703", 
        "description": "A craniosyntosis characterized by autosomal dominant inheritance,  uni- or bicoronal synostosis, macrocephaly, midfacial hypoplasia, and developmental delay that has_material_basis_in a pro250 to agr (P250R) heterozygous mutation in the FGFR3 gene on chromosome 4p16.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060703", 
        "name": "Muenke Syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060703#disease-associations", 
            "id": "0060703", 
            "database": "Alliance of Genome Resources"
        }
    ]
}