{
    "disease_id": "DOID:0111788",
    "recommended_name": {
        "id": "DOID:0111788",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111788",
        "name": "Melnick-Needles syndrome",
        "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 the FLNA gene on chromosome Xq28."
    },
    "synonyms": [
        {
            "id": "DOID:0111788",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111788",
            "name": "MNS",
            "description": ""
        },
        {
            "id": "DOID:0111788",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111788",
            "name": "Melnick-Needles osteodysplasty",
            "description": ""
        },
        {
            "id": "DOID:0111788",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111788",
            "name": "osteodysplasty of Melnick and Needles",
            "description": ""
        },
        {
            "id": "MONDO:0010650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010650",
            "name": "Melnick-Needles syndrome",
            "description": "A otopalatodigital syndrome spectrum disorder and is associated with a short stature, facial dysmorphism, osseous abnormalities involving the majority of the axial and appendicular skeleton resulting in impaired speech and masticatory problems."
        },
        {
            "id": "MONDO:0010650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010650",
            "name": "Melnick Needles Syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010650",
            "name": "Melnick-Needles osteodysplasty",
            "description": ""
        },
        {
            "id": "MONDO:0010650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010650",
            "name": "Melnick-Needles syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010650",
            "name": "Melnick-Needles syndrome, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010650",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010650",
            "name": "MNS",
            "description": ""
        },
        {
            "id": "MIM:309350",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/309350",
            "name": "Melnick-Needles syndrome",
            "description": "Melnick-Needles syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111788"
    ],
    "unlinked_id_list": []
}