{
    "disease_id": "DOID:0111331", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013352", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013352", 
            "name": "FOXP1 related global developmental delay, intellectual disability and speech defects"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013352", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013352", 
            "name": "intellectual disability with language impairment and with or without autistic features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013352", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013352", 
            "name": "mental retardation with language impairment and with or without autistic features"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111331", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111331", 
            "name": "FOXP1 syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111331", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111331", 
            "name": "Mental retardation with language impairment and with or without autistic features"
        }, 
        {
            "url": "https://www.omim.org/entry/613670", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613670", 
            "name": "Mental retardation with language impairment and autistic features"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111331", 
        "description": "A syndromic intellectual disability characterized by global developmental delay with moderate to severe speech delay, dysmorphic craniofacial features, and gross motor skill delays that particularly affects expressive speech that has_material_basis_in heterozygous mutation in FOXP1 on chromosome 3p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111331", 
        "name": "intellectual disability-severe speech delay-mild dysmorphism syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613670", 
            "id": "613670", 
            "database": "MIM"
        }
    ]
}