{
    "disease_id": "DOID:0070421",
    "recommended_name": {
        "id": "DOID:0070421",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070421",
        "name": "neurodevelopmental disorder with spasticity and poor growth",
        "description": "An autosomal recessive intellectual developmental disorder characterized by axial hypotonia, delayed psychomotor development, poor feeding, and failure to thrive with onset in early infancy that has_material_basis_in homozygous mutation in the UFC1 gene on chromosome 1q23."
    },
    "synonyms": [
        {
            "id": "DOID:0070421",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070421",
            "name": "NEDSG",
            "description": ""
        },
        {
            "id": "MONDO:0060752",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060752",
            "name": "neurodevelopmental disorder with spasticity and poor growth",
            "description": ""
        },
        {
            "id": "MONDO:0060752",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060752",
            "name": "neurodevelopmental disorder with spasticity and poor growth",
            "description": ""
        },
        {
            "id": "MONDO:0060752",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060752",
            "name": "NEDSG",
            "description": ""
        },
        {
            "id": "MIM:618076",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618076",
            "name": "Neurodevelopmental disorder with spasticity and poor growth",
            "description": "Neurodevelopmental disorder with spasticity and poor growth"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070421"
    ],
    "unlinked_id_list": []
}