{
    "disease_id": "DOID:0111788", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010650", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010650", 
            "name": "osteodysplasty of Melnick and Needles"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010650", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010650", 
            "name": "MNS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010650", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010650", 
            "name": "Melnick-Needles osteodysplasty"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010650", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010650", 
            "name": "MELNICK-NEEDLES syndrome; MNS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111788", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111788", 
            "name": "MNS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111788", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111788", 
            "name": "Melnick-Needles osteodysplasty"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111788", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111788", 
            "name": "osteodysplasty of Melnick and Needles"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111788", 
        "description": "An otopalatodigital syndrome spectrum disorder characterized by short stature, facial dysmorphism, osseous abnormalities involving the majority of the axial and appendicular skeleton resulting in impaired speech and masticatory problems that has_material_basis_in heterozygous or hemizygous mutation in FLNA on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111788", 
        "name": "Melnick-Needles syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111788#disease-associations", 
            "id": "0111788", 
            "database": "Alliance of Genome Resources"
        }
    ]
}